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WARNING LETTER
•Gilman Cheese Corporation•April 21, 2011

Gilman Cheese Corporation – FDA Warning Letter, Apr 21, 2011

Record Details

The FDA conducted an inspection of Gilman Cheese Corporation's low-acid and acidified food manufacturing facility from April 13-21, 2011. The inspection revealed significant deviations from the Low-Acid Canned Foods (LACF) regulations (21 CFR 113), which are mandatory for manufacturers of such products.

Key violations include: 1. **Failure to file scheduled processes:** The firm manufactures several pasteurized processed cheese products (with onion, jalapeno, and plain cheese food) that are not covered under their currently filed scheduled process with the FDA, violating 21 CFR 108.35(c)(2). 2. **Inaccessible scheduled processes:** The processes and retort venting procedures, including the scheduled process, were not posted near equipment or readily available to operators and lab technicians, violating 21 CFR 113.87. The Quality Assurance Manager was also unaware of a filed process. 3. **Failure to record critical factors:** The firm is not monitoring and recording the amount of a critical factor, (b)(4), in shelf-stable pasteurized processed cheese products, as specified by their process authority, violating 21 CFR 113.100(a). 4. **Inadequate container coding:** Sealed containers are not marked with a code identifying the establishment, product, year, day, and period packed, as required by 21

Company
Gilman Cheese Corporation
Inspection date
April 21, 2011
Product type
Food
Office
Minneapolis District Office
Person
  • Gerald J. Berg
View Company Profile

ID · a8c8a7e0-5e81-432f-aa05-943d56551122

Violation Codes10
21 CFR 11321 CFR 10821 U.S.C. 34421 U.S.C. 342(a)(4)21 CFR 108.35(c)(2)21 CFR 113.8321 CFR 113.8721 CFR 113.100(a)21 CFR 113.60(c)21 CFR 110

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