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Food > Honey > Honey Establishment Inspection Manual > Chapter 5 - Manufacturing Controls 

CHAPTER 5 - MANUFACTURING CONTROLS

5.1 MANUFACTURING CONTROLS
5.1.1 PRODUCT FORMULATION
5.1.1.1 Label Accuracy*
5.1.2 INCOMING MATERIAL CONTROL
5.1.2.1 Ingredients/Additives & Processing Aids*
5.1.2.2 Empty Container Controls (Bulk/Retail)
5.1.3 IN-PROCESS PACKAGE CONTROL
5.1.3.1 Empty Container Handling (Bulk/Retail)*
5.1.4 PRODUCT PREPARATION AND BLENDING CONTROLS
5.1.4.1 Honey Batching and Blending
5.1.5 FILLING CONTROL
5.1.5.1 Filling of Containers
5.1.6 CONTAINER CLOSURE CONTROL
5.1.6.1 Container Closer
5.1.7 PROCESS CONTROL
5.1.7.1 Control of Filling and Labelling
APPENDICES PRODUCER PROGRAM OUTLINES
Appendix 1 Incoming Honey and Ingredients Controls
Appendix 2 Bulk Empty Container Program

* Tasks marked with an asterisk are the ones that have the possibility to be rated with a Category I risk which corresponds to the highest level of risk.

5.1 MANUFACTURING CONTROLS
5.1.1 PRODUCT FORMULATION
5.1.1.1 Label Accuracy
5101 Task
PRINCIPLE The establishment ensures that the label information accurately represents the composition of the food.
Assessment Criteria Procedures are in place to ensure that all labels accurately represent product formulation, composition and claims especially where allergens or ingredients which may cause sensitivities are used.

Allergens include milk, eggs, fish, crustaceans, shell fish, tree nuts, peanuts, soy, wheat, sulphites, sesame seed.

Ingredients which may cause sensitivities include lactose, MSG (monosodium glutamate).

The following are examples of such procedures:

  • New label review
  • Incoming label review for accuracy/correctness
  • Formulation changes/substitutions
Rating Examples
I Omission of allergens in list of ingredients with a known history of producing anaphylactic reaction in sensitive individuals.
II Inadequate or no control of label accuracy and listed ingredients which may cause sensitivities are used in the establishment.
III Use of labels with inaccurate ingredient listings but no listed allergens used in the plant

Inadequate control of label accuracy (e.g. no new label review but no listed allergens used in the plant).

Reference Food Safety Enhancement Program Manual - Chapter 2 Developing a HACCP System - Section 4 - Developing HACCP plan(s)
http://www.inspection.gc.ca/english/fssa/polstrat/haccp/manue/ch2sec3-45e.shtml#2.4

Honey Regulations: Sections 5(1); 5.1; 6; 7; 8; 21(1)(b); 25(a); 34(a), (b) and (d); 35(1), (2), (3), (4) and (5); 36(1), (2) and (3); 37(1), (2) and (3); 52(1) and (2); Schedule I Table I, II, III, IV.
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

 

5.1 MANUFACTURING CONTROLS
5.1.2 INCOMING MATERIAL CONTROL
5.1.2.1 Ingredients/Additives and Processing Aids
5301 Task
PRINCIPLE The establishment controls honey, incoming ingredients, food additives and processing aids such that no biological, physical or chemical hazards result in the food.
Assessment Criteria The establishment controls incoming honey, incoming ingredients, food additives and processing aids through a program consisting of:
  • Written specifications for honey, incoming ingredients, food additives and processing aids. Specifications include a provision for compliance with the Food and Drugs Act and Regulations.
  • The requirements for a letter of guarantee from the supplier.
  • Monitoring and testing to verify adherence to specifications.

The establishment that extracts honey must ensure that:

  • Medications used have been approved for use for treating bees.
  • The recommended preparation and dosage level of the medications have been followed.
  • The withdrawal time for the medication has been followed before the honey is harvested.
  • Records are kept for all applications of treatments to the colonies (e.g. medications, colony evacuation for honey removal, mite control).
Rating Examples
I Use of adulterated/contaminated honey, incoming ingredients, food additives or processing aids.

Medications used for treating bees are not approved.

Dosages and/or withdrawal times for medications have not been followed.

II No letter of guarantee from suppliers for honey, incoming ingredients, food additives and processing aids to indicate regulatory compliance.

The establishment has specifications for critical ingredients but cannot demonstrate adherence (refer to allergen list).

No program or documentation to verify adherence to specifications for all applications of treatments to the colonies (e.g. medications, colony evacuation for honey removal, mite control).

III No specifications for non-critical ingredients (e.g. mustard, flavours).
Reference Honey Regulations: Sections 16(f), 4.1(1).
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

Food and Drug Regulations
http://laws.justice.gc.ca./en/F-27/C.R.C.-c.870/124782.html#rid-124825

Appendix 1 - Incoming Honey and Ingredient Controls.

 

5.1 MANUFACTURING CONTROL
5.1.2 INCOMING MATERIAL CONTROL
5.1.2.2 Empty Container Controls (Bulk /Retail)
5302 Task
PRINCIPLE The establishment controls incoming and outgoing empty containers (bulk/retail) such that no biological, physical or chemical hazard results in the food and to ensure regulatory compliance.
Assessment Criteria Empty containers are evaluated to ensure that specifications are met and containers are free from defects. Verification may be accomplished through review of the supplier's internal audits and through vendor audits.

Packaging materials/containers in use for foods must comply with Division 23 of the Food and Drug Regulations and the Honey Regulations.

Every container for honey shall be in clean, sanitary and sound condition and have a tightly fitting lid.

In addition all bulk containers shall be free from severe dents or buckling and from obvious signs of internal rusting.

Every container for prepackaged honey shall be new.

All empty containers are adequately protected from contamination and damage upon arrival and departure.

Containers are only used for their intended purpose.

Rating Examples
I N/A
II Packaging material/containers does not comply with Division 23 of the Food and Drugs Regulations.

Container is not free from severe dents or buckling.

Containers are not only used for their intended purpose.

III Evaluation-monitoring is not done as scheduled to verify adherence to specifications.

Packaging material/containers does not comply with the Honey Regulations (e.g. non-standard container sizes).

Empty containers are not adequately protected from contamination and damage.

Reference Honey Regulations: Sections 16(b) and (f), 25(d), 29, 30, 32(1) and (2), 33.
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

Food and Drug Regulations: Division 23.
http://laws.justice.gc.ca./en/F-27/C.R.C.-c.870/124782.html#rid-124825

Appendix 1 - Bulk Empty Container Program

 

5.1 MANUFACTURING CONTROL
5.1.3 IN-PROCESS PACKAGE CONTROL
5.1.3.1 Empty Container Handling (Bulk/Retail)
5401 Task
PRINCIPLE Empty container handling is controlled to minimize damage and to prevent the use of damaged, defective or contaminated containers.
Assessment Criteria Containers are handled, transferred and cleaned (when necessary) in a manner that minimizes damage and contamination (e.g. conveyors, transfer points etc.).

The establishment has in place an effective cleaning system.

The establishment has an effective system in place to prevent the use of damaged or defective containers. This can be accomplished by ensuring that:

  • Empty containers are visually or electronically examined to identify, remove and segregate defective containers during depalletizing or on-line
  • There is a back-up system in place in case the electronic inspection system fails
  • The establishment has controls in place to prevent contamination of clean containers. For example:

    - No containers and lids are left on the line at breaks, during clean-up or extended downtime unless adequate measures are in place to prevent contamination.
    - Containers are used only for their intended purpose.

Rating Examples
I Glass particles/fragments detected in open containers or in finished products.
II Containers being used with evidence of major contamination with objectionable material.

Deficiencies in the container handling control program which may result in use of seriously damaged containers.

Containers are not used for their intended purpose.

III No continuous visual monitoring (e.g. no exterior pallet exam prior to depalletizing), however, other visual inspection assessment criteria are satisfactory.

The container handling damage control or visual monitoring program is absent or deficient such that defective containers may be used.

Containers being used with evidence of contamination.

Reference Honey Regulations: Sections 4.1(4), 32, 33.
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

Appendix 2 - Bulk Empty Container Program.

 

5.1 MANUFACTURING CONTROLS
5.1.4 PRODUCT PREPARATION AND BLENDING CONTROLS
5.1.4.1 Honey Batching and Blending
5501 Task
PRINCIPLE Factors for each specific batch/lot are controlled during blending to ensure specified requirements in the Honey Regulations are met.
Assessment Criteria The establishment has controls in place to ensure that the composition of the honey in each batch/lot has been accurately evaluated. Areas which require evaluation are:
  • Colour
  • Moisture
  • Absence of Foreign Material
  • Characteristic Flavour
  • Floral Source (if declared)
  • Lot numbers
  • Country of Origin

The establishment has signed verifications of all batch/lot evaluations

The owner or operator of each registered establishment shall keep and make available to the CFIA at all times, an accurate, up-to-date record of his honey pack that shows:

  • The quantity of honey pooled or purchased and the persons from whom it was received or purchased.
Rating Examples
I N/A
II N/A
III The establishment has no controls and documentation in place for batch/lot blending.

Evaluations performed but no signed verification.

Incomplete/inaccurate evaluations of each batch.

Reference Honey Regulations: Sections 4.1(1), 5, 5.1, 6, 7, 8, 21(1)(a)(ii).
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

 

5.1 MANUFACTURING CONTROLS
5.1.5 FILLING CONTROL
5.1.5.1 Filling of Containers
5601 Task
PRINCIPLE Controls are in place to prevent damage or contamination of containers, lids and product during the filling process.
Assessment Criteria The establishment has controls in place to prevent hazards associated with product filling.

The establishment has controls in place to prevent contamination of clean containers and product, for example:

  • Filled containers without lids are not left on the line at breaks, during clean-up or extended downtime unless adequate measures are in place to prevent contamination.
Rating Examples
I N/A
II Filled containers left on the line during breaks, clean-up, downtime where there is a high risk of contamination.

The establishment does not have adequate controls in place to prevent hazards associated with product filling (glass).

III Filled containers left on the line at breaks and downtime where there is a low to moderate risk of contamination.

The damaged container control or visual monitoring program is absent or deficient such that defective containers may be used.

The establishment does not have adequate controls in place to prevent hazards associated with product filling.

Reference FSEP Manual: Volume II, Ch 4, Application of HACCP.
http://laws.justice.gc.ca./en/F-27/C.R.C.-c.870/124782.html#rid-124825

 

5.1 MANUFACTURING CONTROLS
5.1.6 CONTAINER CLOSURE CONTROL
5.1.6.1 Container Closure
5701 Task
PRINCIPLE Container closure controls are in place to prevent contamination of the food.
Assessment Criteria The establishment controls the closing equipment to ensure the integrity of the container by:
  • Protecting the cap/lid hopper from contamination
  • Adjusting closing equipment to avoid damage to containers
  • Adequate container closure.
Rating Examples
I N/A
II Harmful extraneous material found in capping hopper or capper.
III Capping area not inspected regularly for potential contamination.

Inadequate container closure.

Reference Honey Regulations: Sections 4.1(1)(a), (b), (c), (d) and (e); 4.1(4).
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

 

5.1 MANUFACTURING CONTROLS
5.1.7 PROCESS CONTROL
5.1.7.1 Control of Filling and Labelling
5801 Task
PRINCIPLE The establishment has controls in place to prevent mislabelling and improper filling.
Assessment Criteria The establishment has controls in place to prevent mislabelling and improper filling of containers.

Typical controls should be:

  • Container size for product to be sold in Canada.
  • Effective separation of products during changeovers with records.
  • At the labeler different product labels are effectively separated and the number of product label types are kept to a minimum.
  • Tops and bottoms of label bundles are visually checked for mixed labels prior to use.
  • Prevention of mixing of individual or bundles of labels during storage e.g. storage in separate boxes, no loose labels, and ensuring that unused labels are returned to the correct boxes.
  • Effective weight control system to ensure proper filling at the declared weight.
  • Effective grading system to ensure correct grade evaluations.
Rating Examples
I N/A
II N/A
III Use of incorrect labels or inadequate control of label application.

No effective weight verification system in place.

No effective grade evaluation system in place.

Reference Honey Regulations: Sections 5, 6, 7, 8, 29, 30, 31, 32, 33, 34, 35, 36, 37.
http://laws.justice.gc.ca/en/C-0.4/C.R.C.-c.287/index.html

Appendix 1 - Incoming Honey & Ingredients Program

The establishment controls incoming honey and ingredients (food additives and processing aids) through a program consisting of:

  • Written specifications for honey, incoming ingredients (food additives and processing aids). Specifications include a provision for compliance with the Food and Drugs Act and Regulations.
  • The requirements for a letter of guarantee from the supplier.
  • Monitoring and testing to verify adherence to specifications.

The establishment that extracts honey must ensure that:

  • Medications used have been approved for use for treating bees.
  • The recommended preparation and dosage level of the medications have been followed.
  • The withdrawal time for the medication has been followed before the honey is harvested.
  • Records are kept for all applications of treatments to the colonies (e.g. medications, colony evacuation for honey removal, mite control).

For more information refer to:

Labelling of Foods Causing Allergies and Sensitivities, Canadian Food Inspection Agency.
http://www.inspection.gc.ca/english/fssa/labeti/allerg/allerge.shtml

"Reference Listing Of Accepted Construction Materials, Packaging Materials And Non Food Chemical Products, Policy, Planning & Coordination Directorate, Canadian Food Inspection Agency."
http://www.inspection.gc.ca/english/ppc/reference/cone.shtml

  ASSESSMENT CRITERIA Check if Complete Comments if incomplete or N/A
WHAT The establishment controls incoming honey and ingredients (food additives and processing aids). checkbox  
HOW 1. Written specifications for honey and incoming ingredients (food additives and processing aids). checkbox  
2. Specifications are in compliance with the Food and Drugs Act and Regulations (e.g. contaminants and adulterants). checkbox  
3. A letter of guarantee from the supplier,
Monitoring and testing to verify adherence to specifications.
checkbox  
The establishment that extracts honey must ensure that:

1. Medications used have been approved for use for treating bees.

checkbox  

2. The recommended preparation and dosage level of the medications have been followed.

checkbox  

3. The withdrawal time for the medication has been followed before the honey is harvested.

checkbox  

4. Records are kept for all applications of treatments to the colonies (e.g. medications, colony evacuation for honey removal, mite control.)

checkbox  
FREQUENCY Per shipment or per colony checkbox  
WHO Establishment contact (Manager, Owner) checkbox  

DATE:__________________________________________________________________

SIGNATURE:____________________________________________________________


Appendix 2 - Bulk Empty Container Program

OBJECTIVE:

Bulk containers used in packing honey are received/unloaded, handled, emptied and stored such that they:

  • are clean,
  • are sanitary,
  • are of sound condition,
  • have tightly fitting lids,
  • are free of severe dents or buckling, and
  • have no obvious signs of internal rusting.

PROCEDURE:

Establishment has written procedures for:

  1. Cleaning, handling, storing and using of bulk containers received (Sanitation & Pest Control Program).
  2. Eliminating unsanitary conditions or circumstances as might contaminate a bulk container with dirt or filth or render honey injurious to health.
  3. Checking bulk containers to ensure that they are in sound condition for storing honey.
  4. Fitting lids tightly onto bulk containers.
  5. Checking bulk containers for severe dents or buckling to prevent usage for storing honey.
  6. Checking bulk containers for obvious signs of internal rusting to prevent usage for storing honey.
  7. A designated person or persons are responsible for carrying out the procedures for checking bulk containers to meet the objectives.
  8. Bulk containers that do not meet any of the objectives may either be disposed, reconditioned to meet the objectives or marked to ensure that they are not used to store honey.

CONTROLS:

The establishment has controls in place to ensure that the person responsible checked every bulk container and that bulk containers not meeting objectives are either disposed, reconditioned and/or marked to prevent usage for storing honey.

  ASSESSMENT CRITERIA Check if Complete Comments if incomplete
WHAT The establishment has controls in place for empty containers (bulk/retail) such that no biological, physical or chemical hazards result in the food and to ensure regulatory compliance. checkbox  
HOW The establishment has written procedures for:

1. Cleaning, handling, storing and using of bulk containers received.

checkbox  
2. Eliminating unsanitary conditions or circumstances as might contaminate a bulk container with dirt or filth or render honey injurious to health. checkbox  
3. Checking bulk containers to ensure that they are in sound condition for storing honey. checkbox  
4. Fitting lids tightly onto bulk containers. checkbox  
5. Checking bulk containers for severe dents or buckling to prevent usage for storing honey. checkbox  
6. Checking bulk containers for obvious signs of internal rusting to prevent usage for storing honey. checkbox  
7. Designating a person responsible for carrying out the procedures for checking bulk containers. checkbox  
8. Bulk containers that do not meet conditions of 4, 5 and 6 may either be disposed, reconditioned to meet the conditions of 4, 5 and 6 or marked to ensure that they are not used to store honey. checkbox  
FREQUENCY Continuous monitoring checkbox  
WHO Establishment contact (Manager, Owner) checkbox  

DATE:__________________________________________________________________

SIGNATURE:____________________________________________________________



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