FDA Inspection 920723 — Olympus Corporation of the Americas

Olympus Corporation of the Americas — FEI 2429304

The FDA completed an inspection of Olympus Corporation of the Americas on April 1, 2015 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
April 1, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Center Valley, PA (United States)