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FDA Inspection 1142130 — Nihon Kohden America LLC

Nihon Kohden America LLC — FEI 2080783

The FDA completed an inspection of Nihon Kohden America LLC on May 3, 2021 in Irvine, CA. 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
May 3, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 1252486 (VAI Fri Oct 04 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1088972 (VAI Tue Apr 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1040786 (NAI Thu Oct 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876623 (VAI Thu Apr 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources