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FDA Inspection 709142 — Olympus Corporation Of The Americas

Olympus Corporation Of The Americas — FEI 2429304

The FDA completed an inspection of Olympus Corporation Of The Americas on Feb 10, 2011 in Center Valley, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 10, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Center Valley, PA (United States)

Facility

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FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.