FDA Inspection 1115308 — Tecomet Inc.

Tecomet Inc. — FEI 3005226664

The FDA completed an inspection of Tecomet Inc. on January 13, 2020 in Wilmington, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 13, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wilmington, MA (United States)

Citations

IDCFRDescription
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities