FDA inspection
Sirtex Germany Manufacturing GmbH: FDA inspection ending Apr 25, 2019
FDA inspection 1092889 · No Action Indicated (NAI) · Frankfurt Am Main
Key facts
| Inspection ID | 1092889 |
|---|---|
| Firm | Sirtex Germany Manufacturing GmbH |
| FEI number | 3013070673 |
| Address | Industriepark Hochst, Building G 808 |
| City | Frankfurt Am Main |
| Country | Germany |
| Fiscal year | 2019 |
| Inspection end date | Apr 25, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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