FDA Inspection 837843 — Trinity Medical Devices, Inc.

Trinity Medical Devices, Inc. — FEI 3010042047

The FDA completed an inspection of Trinity Medical Devices, Inc. on Jun 24, 2013 in Morristown, NJ. 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
Jun 24, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Morristown, NJ (United States)

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