FDA inspection
Sofradim Production: FDA inspection ending Jan 22, 2009
FDA inspection 571542 · No Action Indicated (NAI) · Trevoux
Key facts
| Inspection ID | 571542 |
|---|---|
| Firm | Sofradim Production |
| FEI number | 3003521774 |
| Address | 116 Avenue De Formans |
| City | Trevoux |
| Country | France |
| Fiscal year | 2009 |
| Inspection end date | Jan 22, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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