FDA inspection
Abbott GmbH: FDA inspection ending Jun 13, 2013
FDA inspection 839385 · No Action Indicated (NAI) · Wiesbaden
Key facts
| Inspection ID | 839385 |
|---|---|
| Firm | Abbott GmbH |
| FEI number | 3002809144 |
| Address | Max-Planck-Ring 2 |
| City | Wiesbaden |
| Country | Germany |
| Fiscal year | 2013 |
| Inspection end date | Jun 13, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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