FDA inspection
Cellavision AB: FDA inspection ending Jun 5, 2008
FDA inspection 528035 · Voluntary Action Indicated (VAI) · Lund
Key facts
| Inspection ID | 528035 |
|---|---|
| Firm | Cellavision AB |
| FEI number | 3003630693 |
| Address | Forskningsbyn Ideon, Scheelevagen 19a |
| City | Lund |
| Fiscal year | 2008 |
| Inspection end date | Jun 5, 2008 |
| 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