FDA inspection
Cavex Holland B.V.: FDA inspection ending Aug 14, 2008
FDA inspection 539021 · Voluntary Action Indicated (VAI) · Haarlem
Key facts
| Inspection ID | 539021 |
|---|---|
| Firm | Cavex Holland B.V. |
| FEI number | 3008898734 |
| Address | Fustweg 5 |
| City | Haarlem |
| Fiscal year | 2008 |
| Inspection end date | Aug 14, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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