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FDA Inspection 1151279 — Kyocera Medical Technologies, Inc

Kyocera Medical Technologies, Inc — FEI 3007932279

The FDA completed an inspection of Kyocera Medical Technologies, Inc on August 19, 2021 in Redlands, 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
August 19, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Redlands, CA (United States)

Facility

Other inspections at this facility

  • 956387 (OAI Thu Feb 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 915196 (NAI Fri Feb 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 769505 (NAI Thu Feb 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources