FDA inspection
Medart A /S: FDA inspection ending Jun 19, 2003
FDA inspection 280062 · No Action Indicated (NAI) · Hvidovre
Key facts
| Inspection ID | 280062 |
|---|---|
| Firm | Medart A /S |
| FEI number | 3005616124 |
| Address | Industriholmen 15A |
| City | Hvidovre |
| Fiscal year | 2003 |
| Inspection end date | Jun 19, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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