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FDA Inspection 1107356 — Olympus Corporation of the Americas

Olympus Corporation of the Americas — FEI 2429304

The FDA completed an inspection of Olympus Corporation of the Americas on September 26, 2019 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
September 26, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Center Valley, PA (United States)

Facility

Other inspections at this facility

  • 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))
  • 709142 (NAI Thu Feb 10 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources