# FDA WARNING_LETTER - Roy and Louise Noble Dairy Farm - May 26, 2011

Source: https://www.keypedia.com/records/warning_letter/roy-and-louise-noble-dairy-farm/68a526b2-4d9a-4cf3-acdf-945eb6f0241e

> FDA WARNING_LETTER for Roy and Louise Noble Dairy Farm on May 26, 2011. Product: Drugs. Access full analysis and detailed observations.

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## Details

- Record Type: WARNING_LETTER
- Company Name: Roy and Louise Noble Dairy Farm
- Inspection Date: 2011-05-26
- Product Type: Drugs
- Office Name: Department of Health and Human Services
- Summary: On May 26, 2011, the FDA inspected Roy and Louise Noble Dairy Farm, identifying violations of the Federal Food, Drug, and Cosmetic Act. The farm offered for sale an adulterated animal for slaughter as food. Specifically, a bob veal calf sold on February 17, 2011, and slaughtered on February 18, 2011, contained Flunixin in the liver at 2.54 ppm, exceeding the 0.125 ppm tolerance (21 CFR 556.286(b)(i)). It also contained Desfuroylceftiofur in the kidney at 7.3 ppm, exceeding the 0.4 ppm tolerance (21 CFR 556.113(3)(i)). These drug residues caused the food to be adulterated under section 402(a)(2)(C)(ii) of the Act.

Furthermore, the farm held animals under insanitary conditions, failing to maintain treatment records, which could lead to medicated animals with harmful drug residues entering the food supply. This constitutes adulteration under section 402(a)(4) of the Act. The FDA requires prompt corrective action to prevent recurrence, including establishing procedures to ensure compliance. Failure to comply may result in regulatory actions like seizure or injunction. A written response detailing corrective steps must be submitted to the FDA within fifteen working days of receiving

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Company: https://www.keypedia.com/companies/roy-and-louise-noble-dairy-farm/0ab7e80e-590d-44e6-9ef3-a156d6106405

Office: https://www.keypedia.com/offices/department-of-health-and-human-services/cecfcda4-4afa-4a1f-a7b7-a020b79f9861