FDA Inspection 836698 — Benson Medical Instruments Co

Benson Medical Instruments Co — FEI 1000220983

The FDA completed an inspection of Benson Medical Instruments Co on Jun 14, 2013 in Minneapolis, 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
Jun 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Minneapolis, MN (United States)