FDA Inspection 945768 — JVC KENWOOD Corporation

JVC KENWOOD Corporation — FEI 1000207387

The FDA completed an inspection of JVC KENWOOD Corporation on Jul 30, 2015 in Yokohama-shi. 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 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Yokohama-shi (Japan)

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