FDA inspection
PFM Medical Titanium GmbH: FDA inspection ending Jul 9, 2009
FDA inspection 599820 · Voluntary Action Indicated (VAI) · Nuremberg
Key facts
| Inspection ID | 599820 |
|---|---|
| Firm | PFM Medical Titanium GmbH |
| FEI number | 3003936139 |
| Address | Sudwestpark 42 |
| City | Nuremberg |
| Country | Germany |
| Fiscal year | 2009 |
| Inspection end date | Jul 9, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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