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FDA Inspection 966619 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 2183744

The FDA completed an inspection of Isomedix Operations Inc. on April 13, 2016 in Coon Rapids, MN. 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
April 13, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Coon Rapids, MN (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 1217934 (VAI Fri Sep 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060499 (NAI Tue Jul 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 863123 (NAI Tue Jan 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 750179 (NAI Thu Oct 20 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 670424 (NAI Thu Jul 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources