FDA inspection
3M Deutschland GmbH: FDA inspection ending Jan 28, 2010
FDA inspection 649019 · No Action Indicated (NAI) · Seefeld
Key facts
| Inspection ID | 649019 |
|---|---|
| Firm | 3M Deutschland GmbH |
| FEI number | 3002806930 |
| Address | Espe Platz |
| City | Seefeld |
| Country | Germany |
| Fiscal year | 2010 |
| Inspection end date | Jan 28, 2010 |
| 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