FDA inspection
PENTAPHARM AG: FDA inspection ending Feb 20, 2014
FDA inspection 878383 · No Action Indicated (NAI) · Aesch Bl
Key facts
| Inspection ID | 878383 |
|---|---|
| Firm | PENTAPHARM AG |
| FEI number | 1000340866 |
| Address | Dornacherstrasse 112 |
| City | Aesch Bl |
| Country | Switzerland |
| Fiscal year | 2014 |
| Inspection end date | Feb 20, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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