FDA inspection
Gynetics Medical Products NV: FDA inspection ending Aug 9, 2007
FDA inspection 491908 · Voluntary Action Indicated (VAI) · Lommel
Key facts
| Inspection ID | 491908 |
|---|---|
| Firm | Gynetics Medical Products NV |
| FEI number | 3003474731 |
| Address | Rembert Dodoensstraat 51, Kristalpark 3365 |
| City | Lommel |
| Fiscal year | 2007 |
| Inspection end date | Aug 9, 2007 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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