FDA inspection
TriRx Segre: FDA inspection ending Jun 15, 2012
FDA inspection 789010 · Voluntary Action Indicated (VAI) · Segre-En-Anjou Bleu
Key facts
| Inspection ID | 789010 |
|---|---|
| Firm | TriRx Segre |
| FEI number | 1000537829 |
| Address | Segre La Grindoliere, Lieu Dit Cuma |
| City | Segre-En-Anjou Bleu |
| Country | France |
| Fiscal year | 2012 |
| Inspection end date | Jun 15, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
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