FDA Inspection 625039 — Steris Corporation

Steris Corporation — FEI 1043572

The FDA completed an inspection of Steris Corporation on October 28, 2009 in Montgomery, AL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 28, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Montgomery, AL (United States)