FDA Inspection 1211418 — Tecomet Inc

Tecomet Inc — FEI 1000306694

The FDA completed an inspection of Tecomet Inc on Jul 26, 2023 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
Jul 26, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kenosha, WI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.