FDA Inspection
Eurofins PHAST GmbHEurofins PHAST GmbH – FDA Inspection, Dec 13, 2023
Record Details
This FDA Inspection record concerns Eurofins PHAST GmbH, with an inspection on December 13, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- MRA HowardL (Issuing Officer)
View Company Profile
ID · 3dc5c5a4-412f-4bbf-a159-51a47e775dae
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1291084
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Eurofins PHAST GmbH
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 30, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 27, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins PHAST GmbH
- FDA Inspection 1063127 - 2018-07-17
- FDA Inspection 831545 - 2013-04-30
- FDA Inspection 596434 - 2009-05-27
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