FDA inspection
Richard Wolf GmbH: FDA inspection ending Sep 10, 2019
FDA inspection 1106603 · Voluntary Action Indicated (VAI) · Knittlingen
Key facts
| Inspection ID | 1106603 |
|---|---|
| Firm | Richard Wolf GmbH |
| FEI number | 3002808001 |
| Address | Pforzheimer Str. 32 |
| City | Knittlingen |
| Country | Germany |
| Fiscal year | 2019 |
| Inspection end date | Sep 10, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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