FDA Inspection
Intervet GesmbHIntervet GesmbH – FDA Inspection, Mar 10, 2017
Record Details
This FDA Inspection record concerns Intervet GesmbH, with an inspection on March 10, 2017, issued by the Center for Veterinary Medicine, covering veterinary.
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ID · 2af984fe-692f-4a5a-abb9-8f105f73acc5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1009383
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Outcome
- Form 483 issued
FDA Citations
7- 21 CFR 211.194(a)(5)Calculations performed are in the records
- 21 CFR 211.194(a)Complete test data included in records
- 21 CFR 211.194(d)Laboratory equipment calibration records
- 21 CFR 211.204Record information inclusions
- 21 CFR 211.89Quarantine of Rejected Components et. al.
- 21 CFR 211.188(b)Batch production and Batch Control Record Requirements
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of Intervet GesmbH
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 11, 2023 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| February 27, 2015 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| October 13, 2011 | NAI | Center for Veterinary Medicine | Pre-Approval Eval. of Animal Drugs and Food Additives |
Other documents for Intervet GesmbH
- FDA Inspection 1219702 - 2023-05-11
- FDA Inspection 917843 - 2015-02-27
- FDA Inspection 756027 - 2011-10-13
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