FDA inspection
PFM Medical Mepro GMBH: FDA inspection ending Jan 26, 2023
FDA inspection 1198107 · Voluntary Action Indicated (VAI) · Nonnweiler
Key facts
| Inspection ID | 1198107 |
|---|---|
| Firm | PFM Medical Mepro GMBH |
| FEI number | 3005704822 |
| Address | Am Soterberg 4 |
| City | Nonnweiler |
| Country | Germany |
| Fiscal year | 2023 |
| Inspection end date | Jan 26, 2023 |
| 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