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FDA Inspection
•Animart, Inc.•November 13, 2018

Animart, Inc. – FDA Inspection, Nov 13, 2018

Record Details

This FDA Inspection record concerns Animart, Inc., with an inspection on November 13, 2018, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Animart, Inc.
Inspection Date
November 13, 2018
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Julia A. Avery (Issuing Officer)
View Company Profile

ID · 329b2e67-0cf4-4174-a819-32f69f4c0019

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1071522
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 530.41(a)Drugs prohibited for extralabel use in food-producing animal(s)
  2. 21 CFR 530.20(a)(2)(iv)Prescribed ELDU - vet causes an illegal drug residue

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Animart, Inc.

12
DateClassificationOfficeProject area
April 17, 2025Not classifiedMinneapolis District Office
February 15, 2024NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 19, 2024NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
November 7, 2023NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 30, 2023NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 12 other inspections on the company page
Other documents for Animart, Inc.
  • FDA Inspection 1267707 - 2025-04-17
  • FDA Inspection 1231724 - 2024-02-15
  • FDA Inspection 1227717 - 2024-01-19
  • FDA Inspection 1223917 - 2023-11-07
  • FDA Inspection 1223873 - 2023-10-30

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