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WARNING LETTER
•GMC Dairy Farms•March 17, 2015

GMC Dairy Farms – FDA Warning Letter, Mar 17, 2015

Record Details

On March 5 and 17, 2015, the FDA inspected GMC Dairy Farms, identifying violations of the Federal Food, Drug, and Cosmetic Act. The farm offered two adulterated dairy cows for slaughter. One cow, sold around November 12, 2014, had 1.91 ppm of desfuroylceftiofur in its kidney, exceeding the 0.4 ppm tolerance (21 C.F.R. 556.113). Another cow, sold around December 1, 2014, had 3.7 ppm of oxytetracycline in muscle and 12.7 ppm in kidney, exceeding tolerances of 2 ppm and 12 ppm respectively (21 C.F.R. 556.500). These levels caused the food to be adulterated under section 402(a)(2)(C)(ii) of the FD&C Act.

The investigation also found insanitary conditions, including a failure to maintain complete treatment records, leading to adulterated food under section 402(a)(4). Additionally, the new animal drugs Ceftiofur and oxytetracycline were adulterated under section 501(a)(5) because they were used extralabelly without veterinary supervision or adherence to withdrawal times and indications for use, violating 21 C.F.R.

Company
GMC Dairy Farms
Inspection date
March 17, 2015
Product type
Drugs
Office
San Francisco District Office
Person
  • Kathleen M. Lewis
View Company Profile

ID · ac4d9784-566e-4fbf-9995-39635cdb9efc

Violation Codes10
21 U.S.C. 342(a)(2)(C)(ii)21 U.S.C. 360b21 U.S.C. 342(a)(4)21 CFR 556.11321 CFR 556.50021 U.S.C. 360b(a)(4)21 U.S.C. 360b(a)(5)21 CFR 530.3(a)21 CFR 530.11(a)21 CFR 530.11(d)

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