FDA inspection
Tecomet Inc: FDA inspection ending Jun 17, 2004
FDA inspection 334178 · No Action Indicated (NAI) · Kenosha, WI
Key facts
| Inspection ID | 334178 |
|---|---|
| Firm | Tecomet Inc |
| FEI number | 1000306694 |
| Address | 5307 95th Ave |
| City | Kenosha |
| State | WI |
| ZIP | 53144-7494 |
| Fiscal year | 2004 |
| Inspection end date | Jun 17, 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