FDA inspection
Cellavision AB: FDA inspection ending Feb 28, 2013
FDA inspection 822359 · Voluntary Action Indicated (VAI) · Lund
Key facts
| Inspection ID | 822359 |
|---|---|
| Firm | Cellavision AB |
| FEI number | 3003630693 |
| Address | Forskningsbyn Ideon, Scheelevagen 19a |
| City | Lund |
| Country | Sweden |
| Fiscal year | 2013 |
| Inspection end date | Feb 28, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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