FDA inspection
GN Resound North America: FDA inspection ending Nov 14, 2003
FDA inspection 301650 · Voluntary Action Indicated (VAI) · Bloomington, MN
Key facts
| Inspection ID | 301650 |
|---|---|
| Firm | GN Resound North America |
| FEI number | 2182204 |
| Address | 8001 E Bloomington Fwy |
| City | Bloomington |
| State | MN |
| ZIP | 55420-1036 |
| Fiscal year | 2004 |
| Inspection end date | Nov 14, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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