FDA inspection
Eurofins BioPharma Product Testing Spain SLU: FDA inspection ending Jun 19, 2025
FDA inspection 1279238 · No Action Indicated (NAI) · Esplugues De Llobregat
Key facts
| Inspection ID | 1279238 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Spain SLU |
| FEI number | 3007914833 |
| Address | Calle De Josep Argemi 13-15 |
| City | Esplugues De Llobregat |
| Country | Spain |
| Fiscal year | 2025 |
| Inspection end date | Jun 19, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Vaccines and Allergenic 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