FDA inspection
Medart A /S: FDA inspection ending May 11, 2006
FDA inspection 431873 · No Action Indicated (NAI) · Hvidovre
Key facts
| Inspection ID | 431873 |
|---|---|
| Firm | Medart A /S |
| FEI number | 3005616124 |
| Address | Industriholmen 15A |
| City | Hvidovre |
| Fiscal year | 2006 |
| Inspection end date | May 11, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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