FDA inspection
Eurofins BioPharma Product Testing Sweden AB: FDA inspection ending Feb 18, 2011
FDA inspection 725048 · Voluntary Action Indicated (VAI) · Uppsala
Key facts
| Inspection ID | 725048 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Sweden AB |
| FEI number | 3008763211 |
| Address | Rapsgatan 21 |
| City | Uppsala |
| Country | Sweden |
| Fiscal year | 2011 |
| Inspection end date | Feb 18, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
At a glance
- 1–9 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