FDA inspection
Eurofins Biopharma Product Testing Ireland Limited: FDA inspection ending Sep 30, 2009
FDA inspection 618581 · No Action Indicated (NAI) · Dungarvan
Key facts
| Inspection ID | 618581 |
|---|---|
| Firm | Eurofins Biopharma Product Testing Ireland Limited |
| FEI number | 3002807550 |
| Address | Clogherane |
| City | Dungarvan |
| Country | Ireland |
| Fiscal year | 2009 |
| Inspection end date | Sep 30, 2009 |
| 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