FDA inspection
Rexton, A Division of Siemens Hearing Instruments, Inc.: FDA inspection ending Jan 29, 2014
FDA inspection 902256 · No Action Indicated (NAI) · Plymouth, MN
Key facts
| Inspection ID | 902256 |
|---|---|
| Firm | Rexton, A Division of Siemens Hearing Instruments, Inc. |
| FEI number | 1419512 |
| Address | 5010 Cheshire Ln N, Suite 2 |
| City | Plymouth |
| State | MN |
| ZIP | 55446 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Jan 29, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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