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FDA Inspection 750179 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 2183744

The FDA completed an inspection of Isomedix Operations Inc. on October 20, 2011 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
October 20, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Coon Rapids, MN (United States)

Facility

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  • 863123 (NAI Tue Jan 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources