FDA Inspection 753048 — Oxicheck Northwest

Oxicheck Northwest — FEI 3003911103

The FDA completed an inspection of Oxicheck Northwest on Nov 1, 2011 in Bisbee, AZ. 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
Nov 1, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bisbee, AZ (United States)