FDA inspection
Prothya Biosolutions Netherlands B.V.: FDA inspection ending May 13, 2016
FDA inspection 969120 · Voluntary Action Indicated (VAI) · Amsterdam
Key facts
| Inspection ID | 969120 |
|---|---|
| Firm | Prothya Biosolutions Netherlands B.V. |
| FEI number | 3007166802 |
| Address | Plesmanlaan 125 |
| City | Amsterdam |
| Country | Netherlands |
| Fiscal year | 2016 |
| Inspection end date | May 13, 2016 |
| 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
- 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