FDA inspection
Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.: FDA inspection ending Apr 16, 2019
FDA inspection 1090370 · Voluntary Action Indicated (VAI) · Vienna
Key facts
| Inspection ID | 1090370 |
|---|---|
| Firm | Octapharma Pharmazeutika Produktionsgesellschaft m.b.H. |
| FEI number | 3002809097 |
| Address | Oberlaaer Strase 235 |
| City | Vienna |
| Country | Austria |
| Fiscal year | 2019 |
| Inspection end date | Apr 16, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No 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