FDA inspection
Gambro Renal Products, Incorporated: FDA inspection ending Aug 24, 2006
FDA inspection 440468 · No Action Indicated (NAI) · Englewood, CO
Key facts
| Inspection ID | 440468 |
|---|---|
| Firm | Gambro Renal Products, Incorporated |
| FEI number | 1713683 |
| Address | 9540 Maroon Cir Unit 400 |
| City | Englewood |
| State | CO |
| ZIP | 80112-5731 |
| Fiscal year | 2006 |
| Inspection end date | Aug 24, 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