FDA inspection
Eurofins Biopharma Product Testing Switzerland AG: FDA inspection ending Jan 23, 2025
FDA inspection 1268950 · Voluntary Action Indicated (VAI) · Schonenwerd
Key facts
| Inspection ID | 1268950 |
|---|---|
| Firm | Eurofins Biopharma Product Testing Switzerland AG |
| FEI number | 3006749082 |
| Address | Parkstrasse 10 |
| City | Schonenwerd |
| Country | Switzerland |
| Fiscal year | 2025 |
| Inspection end date | Jan 23, 2025 |
| 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