FDA inspection
Prothya Biosolutions Netherlands B.V.: FDA inspection ending Jun 4, 2013
FDA inspection 835110 · Official Action Indicated (OAI) · Amsterdam
Key facts
| Inspection ID | 835110 |
|---|---|
| Firm | Prothya Biosolutions Netherlands B.V. |
| FEI number | 3007166802 |
| Address | Plesmanlaan 125 |
| City | Amsterdam |
| Country | Netherlands |
| Fiscal year | 2013 |
| Inspection end date | Jun 4, 2013 |
| Classification | Official Action Indicated (OAI) |
| 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
- 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