FDA Inspection 951945 — WE Mowrey CO

WE Mowrey CO — FEI 2182977

The FDA completed an inspection of WE Mowrey CO on Dec 9, 2015 in Saint Paul, MN. 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 9, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)