FDA inspection
Willy Rusch GmbH a div of Teleflex Medical: FDA inspection ending Nov 18, 2004
FDA inspection 360481 · No Action Indicated (NAI) · Kernen Im Remstal
Key facts
| Inspection ID | 360481 |
|---|---|
| Firm | Willy Rusch GmbH a div of Teleflex Medical |
| FEI number | 3002808493 |
| Address | Willy-Rusch-Str. 4-10 |
| City | Kernen Im Remstal |
| Fiscal year | 2005 |
| Inspection end date | Nov 18, 2004 |
| 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