FDA inspection
Willy Rusch GmbH a div of Teleflex Medical: FDA inspection ending Jul 18, 2019
FDA inspection 1146119 · Voluntary Action Indicated (VAI) · Kernen Im Remstal
Key facts
| Inspection ID | 1146119 |
|---|---|
| Firm | Willy Rusch GmbH a div of Teleflex Medical |
| FEI number | 3002808493 |
| Address | Willy-Rusch-Str. 4-10 |
| City | Kernen Im Remstal |
| Fiscal year | 2019 |
| Inspection end date | Jul 18, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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