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FDA Inspection 718296 — 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 6, 2011 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 6, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)

Facility

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