FDA Inspection 1116512 — Tecomet, Inc.

Tecomet, Inc. — FEI 3003018882

The FDA completed an inspection of Tecomet, Inc. on January 17, 2020 in Woburn, MA. 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 17, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Woburn, MA (United States)