FDA inspection
Octapharma AB: FDA inspection ending Jan 20, 2011
FDA inspection 710676 · Official Action Indicated (OAI) · Stockholm
Key facts
| Inspection ID | 710676 |
|---|---|
| Firm | Octapharma AB |
| FEI number | 3005559915 |
| Address | Lars Forssells Gata 23 |
| City | Stockholm |
| Country | Sweden |
| Fiscal year | 2011 |
| Inspection end date | Jan 20, 2011 |
| Classification | Official Action Indicated (OAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
| Warning letter | 179372 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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