FDA inspection
Curasan AG, Frankfurt Facility: FDA inspection ending May 11, 2017
FDA inspection 1014030 · Official Action Indicated (OAI) · Frankfurt Am Main
Key facts
| Inspection ID | 1014030 |
|---|---|
| Firm | Curasan AG, Frankfurt Facility |
| FEI number | 3004847139 |
| Address | Ernst-wiss-str. 18 |
| City | Frankfurt Am Main |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | May 11, 2017 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 534581 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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