FDA inspection
GN Resound North America: FDA inspection ending Nov 10, 2004
FDA inspection 356476 · No Action Indicated (NAI) · Bloomington, MN
Key facts
| Inspection ID | 356476 |
|---|---|
| Firm | GN Resound North America |
| FEI number | 2182204 |
| Address | 8001 E Bloomington Fwy |
| City | Bloomington |
| State | MN |
| ZIP | 55420-1036 |
| Fiscal year | 2005 |
| Inspection end date | Nov 10, 2004 |
| 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
- 10–99 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