FDA inspection
Vitrolife Sweden AB: FDA inspection ending Feb 18, 2010
FDA inspection 652647 · No Action Indicated (NAI) · Goteborg
Key facts
| Inspection ID | 652647 |
|---|---|
| Firm | Vitrolife Sweden AB |
| FEI number | 3003995932 |
| Address | Box 9080, Gustaf Werners Gata 2 |
| City | Goteborg |
| Country | Sweden |
| Fiscal year | 2010 |
| Inspection end date | Feb 18, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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