FDA inspection
Angiomed GmbH & Co. Medizintechnik KG: FDA inspection ending Aug 22, 2002
FDA inspection 234927 · No Action Indicated (NAI) · Karlsruhe
Key facts
| Inspection ID | 234927 |
|---|---|
| Firm | Angiomed GmbH & Co. Medizintechnik KG |
| FEI number | 3002806368 |
| Address | Wachhausstr. 6 |
| City | Karlsruhe |
| Fiscal year | 2002 |
| Inspection end date | Aug 22, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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