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FDA Inspection 857844 — Trividia Manufacturing Solutions, Inc.

Trividia Manufacturing Solutions, Inc. — FEI 1210279

The FDA completed an inspection of Trividia Manufacturing Solutions, Inc. on November 26, 2013 in Lancaster, NH. 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
November 26, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Lancaster, NH (United States)

Facility

Other inspections at this facility

  • 1263186 (VAI Thu Mar 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1206742 (NAI Wed May 03 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1071302 (VAI Wed Nov 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1063417 (VAI Fri Aug 24 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1026178 (NAI Wed Aug 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources