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FDA Inspection 724872 — STERIS Corporation

STERIS Corporation — FEI 1937531

The FDA completed an inspection of STERIS Corporation on May 17, 2011 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 17, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
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))
  • 599535 (VAI Thu Jul 16 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

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