FEI establishment
Eurofins Biopharma Product Testing, Denmark A/S
FDA establishment FEI 3006272083 · Glostrup, Denmark
Key facts
| FEI number | 3006272083 |
|---|---|
| Legal name | Eurofins Biopharma Product Testing, Denmark A/S |
| City | Glostrup |
| Country | Denmark |
| Product types | Drugs |
| Drug operations | ANALYSIS |
| Last inspection | May 17, 2023 |
At a glance
- 1–9 FDA inspections
- 1–9 No Action Indicated (NAI)
- 1–9 Voluntary Action Indicated (VAI)
- None Official Action Indicated (OAI)
- 1–9 Inspections with a Form 483
- 10–99 Citations
- 1–9 Repeat citations
- None Warning letters
- None Linked 510(k)s
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA establishments (FEI)
An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection and compliance data