FDA Inspection
Eurofins SF Analytical Laboratories, Inc.Eurofins SF Analytical Laboratories, Inc. – FDA Inspection, Jul 27, 2011
Record Details
This FDA Inspection record concerns Eurofins SF Analytical Laboratories, Inc., with an inspection on July 27, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 27, 2011
- Product Type
- Drugs
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ID · 19808395-3403-45cd-b80f-e65dfa31fd4a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 736116
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
5- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.194(a)Complete test data included in records
- 21 CFR 211.194(a)(7)Signatures and dates--person who performs test
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.182Written records kept in individual logs
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Other FDA inspections of Eurofins SF Analytical Laboratories, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 3, 2026 | Not classified | Philadelphia District Office | Drug Quality Assurance |
| August 9, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins SF Analytical Laboratories, Inc.
- FDA Inspection 1321212 - 2026-06-03
- FDA Inspection 1177148 - 2022-08-09
- FDA Inspection 911124 - 2015-01-22
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