FDA inspection
Integrum Ab: FDA inspection ending May 21, 2015
FDA inspection 926999 · Voluntary Action Indicated (VAI) · Molndal
Key facts
| Inspection ID | 926999 |
|---|---|
| Firm | Integrum Ab |
| FEI number | 3011386779 |
| Address | Krokslatts Fabriker 50 |
| City | Molndal |
| Country | Sweden |
| Fiscal year | 2015 |
| Inspection end date | May 21, 2015 |
| 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