FDA Inspection 756182 — Accutron Inc

Accutron Inc — FEI 2020813

The FDA completed an inspection of Accutron Inc on December 7, 2011 in Phoenix, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 7, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)