FDA Inspection 1037057 — Matthew Warren, Inc.

Matthew Warren, Inc. — FEI 3011445359

The FDA completed an inspection of Matthew Warren, Inc. on Dec 14, 2017 in Southington, CT. 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
Dec 14, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Southington, CT (United States)