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FDA Inspection
•Hunan KYF Pharmaceutical. Co., Ltd•August 16, 2017

Hunan KYF Pharmaceutical. Co., Ltd – FDA Inspection, Aug 16, 2017

Record Details

This FDA Inspection record concerns Hunan KYF Pharmaceutical. Co., Ltd, with an inspection on August 16, 2017, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Hunan KYF Pharmaceutical. Co., Ltd
Inspection Date
August 16, 2017
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Meisha R. Sampson (Issuing Officer)
View Company Profile

ID · edc02bd6-6a48-435a-9785-41161a3d97c9

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1022405
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

Other FDA inspections of Hunan KYF Pharmaceutical. Co., Ltd

4
DateClassificationOfficeProject area
August 11, 2023Not classifiedOffice of Inspections and Investigations
May 27, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 24, 2013VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 19, 2009VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Hunan KYF Pharmaceutical. Co., Ltd
  • FDA Inspection 1218481 - 2023-08-11
  • FDA Inspection 974335 - 2016-05-27
  • FDA Inspection 837533 - 2013-05-24
  • FDA Inspection 584285 - 2009-03-19

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