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FDA Inspection 924246 — Olympus Corporation of the Americas

Olympus Corporation of the Americas — FEI 1000635022

The FDA completed an inspection of Olympus Corporation of the Americas on April 2, 2015 in San Jose, 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
April 2, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

Facility

Other inspections at this facility

  • 1164264 (VAI Thu Mar 10 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1115262 (VAI Fri Jan 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 718296 (NAI Wed Apr 06 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

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