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FDA Inspection 670424 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 2183744

The FDA completed an inspection of Isomedix Operations Inc. on July 1, 2010 in Coon Rapids, MN. 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
July 1, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Coon Rapids, MN (United States)

Facility

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  • 1060499 (NAI Tue Jul 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 966619 (VAI Wed Apr 13 2016 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))

FDA data resources