FDA Inspection 743581 — ARKRAY Factory, Inc.

ARKRAY Factory, Inc. — FEI 3003422726

The FDA completed an inspection of ARKRAY Factory, Inc. on August 4, 2011 in Koka. 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
August 4, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Koka (Japan)