FDA inspection
PENTAPHARM AG: FDA inspection ending Sep 15, 2016
FDA inspection 988595 · Voluntary Action Indicated (VAI) · Aesch Bl
Key facts
| Inspection ID | 988595 |
|---|---|
| Firm | PENTAPHARM AG |
| FEI number | 1000340866 |
| Address | Dornacherstrasse 112 |
| City | Aesch Bl |
| Country | Switzerland |
| Fiscal year | 2016 |
| Inspection end date | Sep 15, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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