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FDA Inspection 950166 — Steris Corporation

Steris Corporation — FEI 1043572

The FDA completed an inspection of Steris Corporation on December 4, 2015 in Montgomery, AL. 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
December 4, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Montgomery, AL (United States)

Facility

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FDA data resources