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FDA Inspection
•Huvepharma Inc.•May 22, 2018

Huvepharma Inc. – FDA Inspection, May 22, 2018

Record Details

This FDA Inspection record concerns Huvepharma Inc., with an inspection on May 22, 2018, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Huvepharma Inc.
Inspection Date
May 22, 2018
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Kellia N. Hicks (FDA Associated Person)
View Company Profile

ID · f4b55241-3eda-41ab-8708-7b06895cea6f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1053387
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

FDA Citations

6
  1. 21 CFR 211.68(b)Computer control of master formula records
  2. 21 CFR 211.25(a)Training , Education , Experience overall
  3. 21 CFR 211.160(a)Following/documenting laboratory controls
  4. 21 CFR 211.192Investigations of discrepancies, failures
  5. 21 CFR 211.22(d)Procedures not in writing, fully followed
  6. 21 CFR 211.80(b)Handling and Storage to Prevent Contamination

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
October 26, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 1, 2015VAICenter 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 997069 - 2016-10-26
  • FDA Inspection 950798 - 2015-09-01

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