FDA Inspection 1037072 — Isomedix Operations, Inc.

Isomedix Operations, Inc. — FEI 1450662

The FDA completed an inspection of Isomedix Operations, Inc. on Nov 30, 2017 in Libertyville, IL. 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
Nov 30, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Libertyville, IL (United States)

Additional Details

Postmarket Audit Inspections

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