FDA inspection
Karl Storz SE & Co. KG: FDA inspection ending May 23, 2002
FDA inspection 218062 · No Action Indicated (NAI) · Tuttlingen
Key facts
| Inspection ID | 218062 |
|---|---|
| Firm | Karl Storz SE & Co. KG |
| FEI number | 3002808268 |
| Address | Mittelstrasse 8, Dr.-Karl-Storz-Str. 34 |
| City | Tuttlingen |
| Fiscal year | 2002 |
| Inspection end date | May 23, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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
- 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