FDA inspection
Eurofins MicroSafe Laboratories: FDA inspection ending Feb 6, 2009
FDA inspection 568486 · Voluntary Action Indicated (VAI) · Leiden
Key facts
| Inspection ID | 568486 |
|---|---|
| Firm | Eurofins MicroSafe Laboratories |
| FEI number | 3004594563 |
| Address | Darwinweg 24 |
| City | Leiden |
| Fiscal year | 2009 |
| Inspection end date | Feb 6, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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