FDA inspection
Perimed AB: FDA inspection ending Feb 11, 2016
FDA inspection 961291 · No Action Indicated (NAI) · Jarfalla
Key facts
| Inspection ID | 961291 |
|---|---|
| Firm | Perimed AB |
| FEI number | 3003244961 |
| Address | Datavagen 9A |
| City | Jarfalla |
| Country | Sweden |
| Fiscal year | 2016 |
| Inspection end date | Feb 11, 2016 |
| 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