FDA Inspection 661409 — Tecomet Inc.

Tecomet Inc. — FEI 3001451451

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