FDA inspection
Byondis BV: FDA inspection ending Nov 17, 2006
FDA inspection 451526 · Voluntary Action Indicated (VAI) · Nijmegen
Key facts
| Inspection ID | 451526 |
|---|---|
| Firm | Byondis BV |
| FEI number | 3002808298 |
| Address | Microweg 22 |
| City | Nijmegen |
| Fiscal year | 2007 |
| Inspection end date | Nov 17, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
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