FDA inspection
Pierre Fabre Medicament Production: FDA inspection ending Sep 10, 2019
FDA inspection 1101981 · Voluntary Action Indicated (VAI) · Idron
Key facts
| Inspection ID | 1101981 |
|---|---|
| Firm | Pierre Fabre Medicament Production |
| FEI number | 3002806390 |
| Address | Avenue de Bearn |
| City | Idron |
| Fiscal year | 2019 |
| Inspection end date | Sep 10, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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