FDA Inspection 1060499 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 2183744

The FDA completed an inspection of Isomedix Operations Inc. on Jul 17, 2018 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 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Coon Rapids, MN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.