FDA inspection
Neoventa Medical AB: FDA inspection ending Feb 10, 2011
FDA inspection 709564 · Voluntary Action Indicated (VAI) · Molndal
Key facts
| Inspection ID | 709564 |
|---|---|
| Firm | Neoventa Medical AB |
| FEI number | 3005011303 |
| Address | Norra Agatan 32 |
| City | Molndal |
| Country | Sweden |
| Fiscal year | 2011 |
| Inspection end date | Feb 10, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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