FDA inspection
Neoventa Medical AB: FDA inspection ending Aug 25, 2005
FDA inspection 393624 · Voluntary Action Indicated (VAI) · Molndal
Key facts
| Inspection ID | 393624 |
|---|---|
| Firm | Neoventa Medical AB |
| FEI number | 3005011303 |
| Address | Norra Agatan 32 |
| City | Molndal |
| Fiscal year | 2005 |
| Inspection end date | Aug 25, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: 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