FDA Inspection 765868 — Tecomet Inc
The FDA completed an inspection of Tecomet Inc on Jan 20, 2012 in Kenosha, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 20, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kenosha, WI (United States)