FDA inspection
Qiagen GmbH: FDA inspection ending Nov 4, 2022
FDA inspection 1197605 · Voluntary Action Indicated (VAI) · Hilden
Key facts
| Inspection ID | 1197605 |
|---|---|
| Firm | Qiagen GmbH |
| FEI number | 3004013603 |
| Address | Qiagen Str. 1 |
| City | Hilden |
| Country | Germany |
| Fiscal year | 2023 |
| Inspection end date | Nov 4, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Project Evaluation: 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