FDA Inspection 669309 — Tecomet, Inc.

Tecomet, Inc. — FEI 3003018882

The FDA completed an inspection of Tecomet, Inc. on May 13, 2010 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
May 13, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Woburn, MA (United States)

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