FDA Inspection 598533 — Fukuda Denshi USA, Inc.

Fukuda Denshi USA, Inc. — FEI 3000215024

The FDA completed an inspection of Fukuda Denshi USA, Inc. on Jul 7, 2009 in Redmond, WA. 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
Jul 7, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redmond, WA (United States)