FDA Inspection 670424 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 2183744

The FDA completed an inspection of Isomedix Operations Inc. on Jul 1, 2010 in Coon Rapids, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 1, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Coon Rapids, MN (United States)

Additional Details

Postmarket Audit Inspections

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