FDA inspection
Prodimed Plastimed Division: FDA inspection ending Mar 12, 2015
FDA inspection 922420 · Voluntary Action Indicated (VAI) · Le Plessis-Bouchard
Key facts
| Inspection ID | 922420 |
|---|---|
| Firm | Prodimed Plastimed Division |
| FEI number | 3003781614 |
| Address | 3 Rue Louis Armand |
| City | Le Plessis-Bouchard |
| Country | France |
| Fiscal year | 2015 |
| Inspection end date | Mar 12, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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