FDA Inspection
Eurofins BioPharma Product Testing Czech Republic s.r.o.Eurofins BioPharma Product Testing Czech Republic s.r.o. – FDA Inspection, Aug 9, 2016
Record Details
This FDA Inspection record concerns Eurofins BioPharma Product Testing Czech Republic s.r.o., with an inspection on August 9, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 9, 2016
- Product Type
- Drugs
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ID · c3e2c10c-50e5-4a31-be1d-0954bd2f1035
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 988104
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Eurofins BioPharma Product Testing Czech Republic s.r.o.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 24, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 16, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 29, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 20, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins BioPharma Product Testing Czech Republic s.r.o.
- FDA Inspection 1270980 - 2024-07-24
- FDA Inspection 1134811 - 2020-07-16
- FDA Inspection 892490 - 2014-07-29
- FDA Inspection 727383 - 2011-05-20
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