FDA inspection
Eurofins Biopharma Product Testing Ireland Limited: FDA inspection ending Jun 20, 2025
FDA inspection 1280309 · No Action Indicated (NAI) · Dungarvan
Key facts
| Inspection ID | 1280309 |
|---|---|
| Firm | Eurofins Biopharma Product Testing Ireland Limited |
| FEI number | 3002807550 |
| Address | Ida Industrial Estate, Clogherane |
| City | Dungarvan |
| Country | Ireland |
| Fiscal year | 2025 |
| Inspection end date | Jun 20, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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