FDA inspection
Eurofins BioPharma Product Testing Spain SLU: FDA inspection ending Jan 13, 2022
FDA inspection 1285158 · Voluntary Action Indicated (VAI) · Esplugues De Llobregat
Key facts
| Inspection ID | 1285158 |
|---|---|
| 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 | 2022 |
| Inspection end date | Jan 13, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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