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FDA Inspection 599535 — STERIS Corporation

STERIS Corporation — FEI 1937531

The FDA completed an inspection of STERIS Corporation on July 16, 2009 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 16, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 1223087 (VAI Mon Nov 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 977303 (NAI Wed Jun 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 915094 (NAI Fri Feb 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 724872 (NAI Tue May 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources