FDA Inspection
Eurofins CDMO Alphora Inc.FDA Inspection 870592 - Eurofins CDMO Alphora Inc. - February 20, 2014
Record Details
This FDA Inspection record concerns Eurofins CDMO Alphora Inc., with an inspection on February 20, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Eurofins CDMO Alphora Inc.
- Inspection Date
- February 20, 2014
- Product Type
- Drugs
View Company Profile
ID · a50f8b9f-75bb-4623-9f50-254a905da4c3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 870592
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Eurofins CDMO Alphora Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 17, 2025 | Not classified | Office of Inspections and Investigations | |
| 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 |
| December 2, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Eurofins CDMO Alphora Inc.
- FDA Inspection 1258608 - 2025-01-17
- FDA Inspection 1106349 - 2019-10-11
- FDA Inspection 972749 - 2016-04-29
- FDA Inspection 757080 - 2011-12-02
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