Welcome to California California Home   DHCS Home    CDPH Home
Link to State of California Home Page Link to Department of Health Care Services Home Page Linkg to California Department of Public Health Home Page
DHCS Home
CDPH Home
Printer Friendly Version

Drug Safety Program
Export Document Program
Organic Processed Products Program
Food Safety Program
Home Medical Device Retail Program
Medical Device Safety Program
S.T.A.K.E. Program
Sherman Food, Drug, and Cosmetic Law (pdf)
Application Instructions and Forms
Consumer Complaints
Comments and Questions


adobe reader free download

The Adobe Reader is required to view several documents contained on this website

Food and Drug Branch

Industry Assistance: Receiving/Storage/Packaging/Transport

When purchasing food ingredients (both raw and processed), management should establish specifications for each of the items that are to be received. The specifications may be that the products meet management’s standards in the areas of quality, temperature, size, and microbiological standards. Processors should evaluate whether the food product purchased was produced at sites that adhere to GMP and meet established specifications.

To ensure that the quality of freshly processed food is not compromised, all transportation equipment carrying these products should be cleaned and sanitized frequently.

Magnified GraphicAt the time of receipt, processors should visually examine the incoming product for rot, decay, foreign objects, and damaged containers. All incoming ingredients must be inspected and be accepted or rejected. In case a traceback is required, processors will need to determine which incoming ingredients are components of which finished product. It is recommended that processors document the following information for traceback purposes, at the time of receipt of an ingredient: type of product; ingredient and product packaging; labeling; lot number; and pallet tag, quantity, size, and weight. There are many ways a firm can document incoming product receipt and tie it to production for better traceback. Maintaining documents in case of a traceback may minimize the public health and economic impact of a recall.

Record keeping practices should be applied to all items that are added to processed food products and to packaging materials. Quality control review of all ingredients and packaging materials is the first step in producing the safest processed food at the facility. Workers involved in the loading and unloading of raw ingredients during transport should practice good personal hygiene and sanitation, as discussed previously.

To minimize potential microbial hazards when receiving product, the buildings, fixtures, other physical facilities, and surrounding grounds should be maintained in good sanitary condition. Pathogenic microorganisms may be found on floors, in drains of packing facilities and on the surfaces of sorting, grading, and packing equipment. Without use of good sanitary practices, surfaces that come into contact with raw ingredients could be a source of microbial contamination. Therefore, good sanitation practices should be used throughout the facility and staging areas to control contamination throughout the receiving, processing, and packing operations.

Packaging containers and other packing materials that are not used right away should be stored in a way that protects them from contamination by pests, dirt, and water condensing from overhead equipment and structures. Packaging materials should:

  • be manufactured from food grade materials,
  • be stored away from any industrial chemicals and other possible contaminants, and
  • not be used to store hazardous chemicals to avoid cross-contamination.

To insure proper rotation of inventory all pallets should be dated upon receipt. Also, an appropriate detailed inventory system should be established in order to insure first-in-first-out (FIFO) use and shipment of product. Similar commodities should be stored together in order to prevent cross-contamination.

All equipment should be maintained in a clean and sanitary condition. All remnants of food products on belts, tables, lines, and conveyors may serve as a source for microbial contamination and should be removed and the equipment cleaned. When knives and cutting equipment, boots, gloves, smocks, and aprons are used during the processing, they should be cleaned on a regular basis or replaced if they become damaged and/or cannot be kept in sanitary condition.

When preparing finished product for shipment to customers, processors are encouraged to examine all transportation vehicles before loading freight carriers or refrigerated trailers with product. Because transportation vehicles can be a potential source of microbial contamination, trailers should be inspected for general condition, obvious contaminants, and odors before loading. Only trailers with no obvious signs of contamination should be loaded. Drivers should be advised to properly clean, sanitize, and repair trailers prior to loading.

To view the FDA’s booklet "Inspecting Incoming Food Materials" click on the following link: www.cfsan.fda.gov/~dms/insp-toc.html

This is only a brief outline of the GMP that are required for processed food. GMP can be useful in helping processors control their process and minimize microbial, chemical and physical hazards during all stages of the processing operation. In addition, some states, including California, have incorporated the GMP regulations into the State Health and Safety Codes making them requirements for all foods produced in the state.

To operate and maintain your business, you must meet the requirements in the GMP. The following documents are the GMP regulations and a checklist that you can use to check and make corrections to ensure all the conditions set forth in the GMP are met. Click on the documents below for a complete guide to GMP and an easy to follow GMP self inspection checklist.

To view a copy of the FDA’s "Do Your Own Establishment Inspection", click on the following link: www.cfsan.fda.gov/~dms/selfinsp.html

A copy of the "Current Good Manufacturing Practice in Manufacturing, Packing or Holding Human Food" regulation can also be obtained by downloading from the FDA website at www.fda.gov.

GMP represent only one important prerequisite program. Other examples of prerequisite programs are Standard Operating Procedures (SOP), Sanitation Standard Operating Procedures (SSOP), operational actions such as raw material controls, product coding and labeling, product traceability and recall procedures, consumer complaint management and crisis management.

Next Standard Operating Procedures and Sanitation Standard Operating Procedures

Return to Table of Contents


Back to Top of Page
© 2007 State of California | Conditions of Use | Privacy Policy