FDA inspection
Qiagen Manchester Ltd.: FDA inspection ending Jan 24, 2020
FDA inspection 1117588 · Voluntary Action Indicated (VAI) · Manchester
Key facts
| Inspection ID | 1117588 |
|---|---|
| Firm | Qiagen Manchester Ltd. |
| FEI number | 3009391812 |
| Address | 4 Skelton House, Lloyd Street North |
| City | Manchester |
| Country | United Kingdom |
| Fiscal year | 2020 |
| Inspection end date | Jan 24, 2020 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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