FDA inspection
PAJUNK GMBH MEDIZINTECHNOLOGIE: FDA inspection ending Jan 31, 2013
FDA inspection 818828 · Voluntary Action Indicated (VAI) · Geisingen
Key facts
| Inspection ID | 818828 |
|---|---|
| Firm | PAJUNK GMBH MEDIZINTECHNOLOGIE |
| FEI number | 3002807847 |
| Address | Karl-hall-str. 1, KARL-HALL-STRASSE 01 |
| City | Geisingen |
| Country | Germany |
| Fiscal year | 2013 |
| Inspection end date | Jan 31, 2013 |
| 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
- Yes 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