FDA Inspection
Fareva AmboiseFareva Amboise – FDA Inspection, May 25, 2018
Record Details
This FDA Inspection record concerns Fareva Amboise, with an inspection on May 25, 2018, issued by the Center for Veterinary Medicine, covering veterinary.
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ID · 852504e0-9dac-4fc6-8be3-cc2c01e51721
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1055251
- FDA center
- Animal Drugs & Feeds
- Project area
- Pre-Approval Eval. of Animal Drugs and Food Additives
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 211.68(b)Computer control of master formula records
- 21 CFR 211.42(a)Buildings of Suitable Size, Construction, Location
- 21 CFR 211.22(a)Approve or reject components, products
- 21 CFR 211.100(a)Absence of Written Procedures
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Other FDA inspections of Fareva Amboise
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 16, 2025 | OAI | Office of Inspections and Investigations | Drug Quality Assurance |
| October 13, 2023 | Not classified | Office of Inspections and Investigations | |
| December 13, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 16, 2017 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| March 18, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Fareva Amboise
- FDA Inspection 1282366 - 2025-09-16
- FDA Inspection 1241012 - 2023-10-13
- FDA Inspection 1100819 - 2018-12-13
- FDA Inspection 1014635 - 2017-05-16
- FDA Inspection 872367 - 2014-03-18
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