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FDA Inspection
•Huvepharma Inc.•June 16, 2011

Huvepharma Inc. – FDA Inspection, Jun 16, 2011

Record Details

This FDA Inspection record concerns Huvepharma Inc., with an inspection on June 16, 2011, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Huvepharma Inc.
Inspection Date
June 16, 2011
Product Type
Veterinary
Office
Center for Veterinary Medicine
View Company Profile

ID · bdda001c-2261-4630-bc75-2a66d1da9e86

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
728225
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

FDA Citations

9
  1. 21 CFR 211.142(b)Storage under appropriate conditions
  2. 21 CFR 211.25(a)Training , Education , Experience overall
  3. 21 CFR 211.142Written warehousing procedures established/followed
  4. 21 CFR 211.42(c)(2)Rejected Material Area
  5. 21 CFR 211.42(c)(7)Quarantined Drug Products Area
  6. 21 CFR 211.125(a)Strict control not exercised over labeling issued
  7. 21 CFR 211.166(a)Written program not followed
  8. 21 CFR 211.67(b)Written procedures fail to include
  9. 21 CFR 211.192Written record of investigation incomplete

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Huvepharma Inc.

9
DateClassificationOfficeProject area
January 17, 2025Not classifiedKansas City District Office
January 30, 2023VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
August 10, 2021VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 22, 2018VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 26, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 9 other inspections on the company page
Other documents for Huvepharma Inc.
  • FDA Inspection 1259199 - 2025-01-17
  • FDA Inspection 1195992 - 2023-01-30
  • FDA Inspection 1148652 - 2021-08-10
  • FDA Inspection 1053387 - 2018-05-22
  • FDA Inspection 997069 - 2016-10-26

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