FDA Inspection
Eurofins BioPharma Product Testing Sweden ABEurofins BioPharma Product Testing Sweden AB – FDA Inspection, Mar 13, 2015
Record Details
This FDA Inspection record concerns Eurofins BioPharma Product Testing Sweden AB, with an inspection on March 13, 2015, issued by the Center for Veterinary Medicine, covering veterinary.
- Inspection Date
- March 13, 2015
- Product Type
- Veterinary
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ID · 4390b5ec-da18-42c5-bfe0-424fa6dfb118
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 920666
- FDA center
- Animal Drugs & Feeds
- Project area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
FDA Citations
3- 21 CFR 211.160(a)Deviations from laboratory control requirements
- 21 CFR 211.194(a)Complete test data included in records
- 21 CFR 211.160(a)Lab controls established, including changes
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Other FDA inspections of Eurofins BioPharma Product Testing Sweden AB
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 8, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 12, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 18, 2011 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Eurofins BioPharma Product Testing Sweden AB
- FDA Inspection 1233031 - 2022-12-08
- FDA Inspection 1016317 - 2017-05-12
- FDA Inspection 725048 - 2011-02-18
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