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FDA Inspection 1016467 — Tecomet Inc

Tecomet Inc — FEI 1000306694

The FDA completed an inspection of Tecomet Inc on January 12, 2017 in Kenosha, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kenosha, WI (United States)

Facility

Other inspections at this facility

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  • 1211418 (NAI Wed Jul 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 765868 (NAI Fri Jan 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 683368 (NAI Wed Oct 13 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources