FDA Inspection 761236 — Nihon Kohden Corp.

Nihon Kohden Corp. — FEI 3002807720

The FDA completed an inspection of Nihon Kohden Corp. on Dec 13, 2011 in Shinjuku. 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
Dec 13, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Shinjuku (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.