FDA inspection
Eurofins Biopharma Product Testing Munich GmbH: FDA inspection ending Sep 12, 2014
FDA inspection 895118 · No Action Indicated (NAI) · Planegg
Key facts
| Inspection ID | 895118 |
|---|---|
| Firm | Eurofins Biopharma Product Testing Munich GmbH |
| FEI number | 3003706029 |
| Address | Robert-Koch-Str. 3a |
| City | Planegg |
| Country | Germany |
| Fiscal year | 2014 |
| Inspection end date | Sep 12, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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