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WARNING LETTER
•R & D Ranch•December 13, 2012

R & D Ranch – FDA Warning Letter, Dec 13, 2012

Record Details

On January 25, 2013, the FDA issued a Warning Letter to Ray F. Christie, owner of R & D Ranch, following an investigation of his calf buying operation conducted on December 10, 12, and 13, 2012. The investigation revealed that seven animals offered for slaughter as food were adulterated under section 402(a)(2)(C)(ii) of the FD&C Act, 21 U.S.C. § 342(a)(2)(C)(ii), due to unsafe new animal drug residues.

Specifically, four bob veal calves sold for slaughter on September 10, September 13, October 15, and October 25, 2012, contained neomycin residues in kidney tissue exceeding the 7.2 ppm tolerance (21 C.F.R. 556.430). Levels detected were 8.11 ppm, 10.21 ppm, 24.38 ppm, and 24.38 ppm, respectively. The calf sold on October 25, 2012, also contained oxytetracycline at 2.24 ppm in muscle tissue, exceeding the 2 ppm tolerance (21 C.F.R. 556.500).

The FDA requires prompt corrective action to

Company
R & D Ranch
Inspection date
December 13, 2012
Product type
Drugs
Office
San Francisco District Office
Person
  • Barbara J. Cassens (Director )
View Company Profile

ID · 5836f7ff-561a-4fd4-8743-d916507bd899

Violation Codes4
21 U.S.C. 342(a)(2)(C)(ii)21 U.S.C. 360b21 CFR 556.43021 CFR 556.500

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