FDA inspection
Eurofins BioPharma Product Testing Leiden B.V.: FDA inspection ending Mar 18, 2013
FDA inspection 823838 · Voluntary Action Indicated (VAI) · Leiden
Key facts
| Inspection ID | 823838 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Leiden B.V. |
| FEI number | 3004939239 |
| Address | Archimedesweg 25 |
| City | Leiden |
| Country | Netherlands |
| Fiscal year | 2013 |
| Inspection end date | Mar 18, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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