FDA inspection
Argene S.A.: FDA inspection ending Nov 13, 2003
FDA inspection 302662 · Voluntary Action Indicated (VAI) · Verniolle
Key facts
| Inspection ID | 302662 |
|---|---|
| Firm | Argene S.A. |
| FEI number | 1000351505 |
| Address | Parc Artisanal Delta Sud, Parc Technologique Delta Sud |
| City | Verniolle |
| Fiscal year | 2004 |
| Inspection end date | Nov 13, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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