FDA inspection
Timm Medical Technologies, Inc.: FDA inspection ending Feb 22, 2007
FDA inspection 460739 · No Action Indicated (NAI) · Eden Prairie, MN
Key facts
| Inspection ID | 460739 |
|---|---|
| Firm | Timm Medical Technologies, Inc. |
| FEI number | 3001237745 |
| Address | 9600 W 76th St Ste T |
| City | Eden Prairie |
| State | MN |
| ZIP | 55344-3789 |
| Fiscal year | 2007 |
| Inspection end date | Feb 22, 2007 |
| 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