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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 February 10, 2011 in Center Valley, PA. 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
February 10, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Center Valley, PA (United States)

Facility

Other inspections at this facility

  • 1107356 (NAI Thu Sep 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 920723 (NAI Wed Apr 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835336 (VAI Fri May 31 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 793907 (OAI Thu Aug 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources