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FDA Inspection 876623 — Nihon Kohden America LLC

Nihon Kohden America LLC — FEI 2080783

The FDA completed an inspection of Nihon Kohden America LLC on April 24, 2014 in Irvine, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 24, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

Facility

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FDA data resources