FDA inspection
Orfit Industries NV: FDA inspection ending Feb 19, 2015
FDA inspection 925777 · Voluntary Action Indicated (VAI) · Wijnegem
Key facts
| Inspection ID | 925777 |
|---|---|
| Firm | Orfit Industries NV |
| FEI number | 1000227792 |
| Address | Vosveld 9a |
| City | Wijnegem |
| Country | Belgium |
| Fiscal year | 2015 |
| Inspection end date | Feb 19, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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