FDA Inspection 845181 — STERIS CORPORATION

STERIS CORPORATION — FEI 3007412809

The FDA completed an inspection of STERIS CORPORATION on July 29, 2013 in Franklin Park, IL. 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
July 29, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Franklin Park, IL (United States)