FDA inspection
Celerion Switzerland AG: FDA inspection ending Feb 15, 2019
FDA inspection 1086045 · No Action Indicated (NAI) · Fehraltorf
Key facts
| Inspection ID | 1086045 |
|---|---|
| Firm | Celerion Switzerland AG |
| FEI number | 3010653440 |
| Address | Ch-8320, Allmendstrasse 32 |
| City | Fehraltorf |
| Country | Switzerland |
| Fiscal year | 2019 |
| Inspection end date | Feb 15, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring |
| 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