FDA inspection
Maquet Critical Care AB: FDA inspection ending Nov 14, 2000
FDA inspection 59763 · No Action Indicated (NAI) · Solna
Key facts
| Inspection ID | 59763 |
|---|---|
| Firm | Maquet Critical Care AB |
| FEI number | 3002808128 |
| Address | Rontgenvagen 2 |
| City | Solna |
| Fiscal year | 2001 |
| Inspection end date | Nov 14, 2000 |
| 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