FDA Inspection
Eurofins CDMO Alphora Inc.FDA Inspection 1258608 - Eurofins CDMO Alphora Inc. - January 17, 2025
Record Details
This FDA Inspection record concerns Eurofins CDMO Alphora Inc., with an inspection on January 17, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b47bfba1-a831-4679-b35d-c4a2b3cb1dd0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1258608
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Eurofins CDMO Alphora Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 11, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 29, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 20, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 2, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins CDMO Alphora Inc.
- FDA Inspection 1106349 - 2019-10-11
- FDA Inspection 972749 - 2016-04-29
- FDA Inspection 870592 - 2014-02-20
- FDA Inspection 757080 - 2011-12-02
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