FDA inspection
Eurofins Biopharma Product Testing, Denmark A/S: FDA inspection ending Dec 14, 2012
FDA inspection 811362 · Voluntary Action Indicated (VAI) · Glostrup
Key facts
| Inspection ID | 811362 |
|---|---|
| Firm | Eurofins Biopharma Product Testing, Denmark A/S |
| FEI number | 3006272083 |
| Address | Ornebjergvej 1 |
| City | Glostrup |
| Country | Denmark |
| Fiscal year | 2013 |
| Inspection end date | Dec 14, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data