FDA inspection
Eurofins Pharmaceutical Product Testing Belgium NV: FDA inspection ending Sep 26, 2017
FDA inspection 1028878 · No Action Indicated (NAI) · Nazareth
Key facts
| Inspection ID | 1028878 |
|---|---|
| Firm | Eurofins Pharmaceutical Product Testing Belgium NV |
| FEI number | 3012626551 |
| Address | Venecoweg 5 |
| City | Nazareth |
| Fiscal year | 2017 |
| Inspection end date | Sep 26, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None 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