FDA inspection
Jolife AB: FDA inspection ending Mar 24, 2010
FDA inspection 659849 · Voluntary Action Indicated (VAI) · Lund
Key facts
| Inspection ID | 659849 |
|---|---|
| Firm | Jolife AB |
| FEI number | 3005445717 |
| Address | Scheelevagen 17, Ideon Science Park |
| City | Lund |
| Country | Sweden |
| Fiscal year | 2010 |
| Inspection end date | Mar 24, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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