FDA Inspection 1116512 — Tecomet, Inc.

Tecomet, Inc. — FEI 3003018882

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

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