Eurofins Biopharma Product Testing, Denmark A/S — FDA Facility Profile
Eurofins Biopharma Product Testing, Denmark A/S is an FDA-registered facility (FEI 3006272083) located in Hovedstaden DK-2600, DK. Registered operations: ANALYSIS. RegDataLab tracks 5 FDA inspections at this facility.
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What FDA found at this site
- Latest inspection
- May 17, 2023: No Action Indicated (NAI)
- Inspections on record
- 5 (3 VAI, 2 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
Inspections and what FDA cited
| Date | Result | What FDA cited |
|---|---|---|
| May 17, 2023 | No Action Indicated (NAI) | No citations listed |
| Jun 22, 2016 | Voluntary Action Indicated (VAI) | Procedures not in writing, fully followed (21 CFR 211.22(d)) Computer control of master formula records (21 CFR 211.68(b)) Complete test data included in records (21 CFR 211.194(a)) Deviations from laboratory control requirements (21 CFR 211.160(a)) and 1 more |
| Dec 14, 2012 | Voluntary Action Indicated (VAI) | No citations listed |
| Mar 30, 2012 | No Action Indicated (NAI) | No citations listed |
| May 12, 2009 | Voluntary Action Indicated (VAI) | No citations listed |
Facility details
- Company
- Eurofins Biopharma Product Testing, Denmark A/S
- Location
- Hovedstaden DK-2600 (DK)
- Registration Expires
- Dec 31, 2026
- Operations
- ANALYSIS
- Source
- decrs