FDA Inspection
Eurofins BioPharma Product Testing ENCO Inc.Eurofins BioPharma Product Testing ENCO Inc. – FDA Inspection, Jul 11, 2014
Record Details
This FDA Inspection record concerns Eurofins BioPharma Product Testing ENCO Inc., with an inspection on July 11, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 11, 2014
- Product Type
- Drugs
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ID · d239bc90-9209-4b66-bb23-2002e02d78be
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 889761
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.25(a)Training , Education , Experience overall
- 21 CFR 211.194(d)Laboratory equipment calibration records
- 21 CFR 212.60(f)Lab written procedures
- 21 CFR 211.160(a)Lab controls established, including changes
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Other FDA inspections of Eurofins BioPharma Product Testing ENCO Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 1, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 12, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 14, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins BioPharma Product Testing ENCO Inc.
- FDA Inspection 1279054 - 2025-08-01
- FDA Inspection 1041344 - 2018-01-12
- FDA Inspection 822786 - 2013-02-14
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