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WARNING LETTER
•Lor-Rob Dairy Farm•August 22, 2012

Lor-Rob Dairy Farm – FDA Warning Letter, Aug 22, 2012

Record Details

On August 15, 17, and 22, 2012, the FDA inspected Lor-Rob Dairy Farm, identifying violations of the Federal Food, Drug, and Cosmetic Act. The farm sold a cow for slaughter on March 29, 2012, which was found to have 0.39 ppm of ampicillin in its kidney, exceeding the 0.01 ppm tolerance (21 C.F.R. 556.40). This rendered the food adulterated under section 402(a)(2)(C)(ii) of the FD&C Act.

The investigation also revealed unsanitary conditions, including a failure to maintain complete treatment records, making food from such animals adulterated under section 402(a)(4). Furthermore, the farm adulterated the new animal drug (b)(4) (ampicillin) by using it extralabelly without following the veterinarian's prescribed duration of treatment, violating 21 C.F.R. 530.11(a). This non-conforming use caused the drug to be unsafe and adulterated under sections 512(a) and 501(a)(5) of the FD&C Act.

Lor-Rob Dairy Farm must take prompt action to correct these violations and establish procedures to prevent recurrence. A written response detailing corrective actions and timelines is required

Company
Lor-Rob Dairy Farm
Inspection date
August 22, 2012
Product type
Drugs
Office
Department of Health and Human Services
Person
  • Ronald M. Pace (Program Director)
View Company Profile

ID · 7810378c-c89b-4e85-8dbd-79f591957f19

Violation Codes10
FD&C Act 402(a)(2)(C)(ii)21 U.S.C. 342(a)(2)(C)(ii)FD&C Act 51221 U.S.C. 360bFD&C Act 402(a)(4)21 U.S.C. 342(a)(4)21 CFR 556.4021 CFR 530.3(a)FD&C Act 512(a)(4)21 U.S.C. 360b(a)(4)

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