FDA inspection
PAJUNK GMBH MEDIZINTECHNOLOGIE: FDA inspection ending Dec 17, 2009
FDA inspection 635485 · No Action Indicated (NAI) · Geisingen
Key facts
| Inspection ID | 635485 |
|---|---|
| Firm | PAJUNK GMBH MEDIZINTECHNOLOGIE |
| FEI number | 3002807847 |
| Address | Karl-hall-str. 1, KARL-HALL-STRASSE 01 |
| City | Geisingen |
| Country | Germany |
| Fiscal year | 2010 |
| Inspection end date | Dec 17, 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