FDA Inspection 920392 — Steris Corporation

Steris Corporation — FEI 1526531

The FDA completed an inspection of Steris Corporation on April 9, 2015 in Middleburg Heights, OH. 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 9, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Middleburg Heights, OH (United States)