FDA inspection
EUROAPI FRANCE: FDA inspection ending Nov 17, 2017
FDA inspection 1067732 · Voluntary Action Indicated (VAI) · Vertolaye
Key facts
| Inspection ID | 1067732 |
|---|---|
| Firm | EUROAPI FRANCE |
| FEI number | 1463 |
| Address | Rue Du Bourg |
| City | Vertolaye |
| Country | France |
| Fiscal year | 2018 |
| Inspection end date | Nov 17, 2017 |
| 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
- 10–99 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