Eurofins CDMO Alphora Inc FDA Inspection Record
Eurofins CDMO Alphora Inc is an FDA-registered facility (FEI 3005804912) located in Mississauga, CA. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 5 FDA inspections at this facility.
What FDA found at this site
- Latest inspection
- Jan 17, 2025: Voluntary Action Indicated (VAI)
- Inspections on record
- 5 (4 VAI, 1 NAI)
- Last OAI inspection
- None on record
- Warning letters
- None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
- Import refusals
- 4
Inspections and what FDA cited
| Date | Result | What FDA cited |
|---|---|---|
| Jan 17, 2025 | Voluntary Action Indicated (VAI) | No citations listed |
| Oct 11, 2019 | Voluntary Action Indicated (VAI) | No citations listed |
| Apr 29, 2016 | No Action Indicated (NAI) | No citations listed |
| Feb 20, 2014 | Voluntary Action Indicated (VAI) | No citations listed |
| Dec 2, 2011 | Voluntary Action Indicated (VAI) | No citations listed |
When each source was last refreshed
| Records | Last refreshed | Source as of | Status |
|---|---|---|---|
| Inspections | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Inspection citations | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions (warning letters, injunctions and other action types) | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
| Warning letter text | Nov 14, 2026 | Newest record Nov 10, 2026 | Current |
| Recalls (Enforcement Report) | Nov 14, 2026 | Newest record Nov 11, 2026 | Current |
| Form 483s and inspection documents | Nov 13, 2026 | Newest record Nov 12, 2026 | Current |
| Import refusals | Nov 2, 2026 | Newest record Oct 22, 2026 | Current |
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Facility details
- Company
- Eurofins CDMO Alphora Inc.
- Location
- Mississauga (CA)
- Registration Expires
- Dec 31, 2027
- Operations
- ANALYSIS; API MANUFACTURE
- Source
- decrs