FDA Inspection 1076625 — Isomedix Operations Inc.

Isomedix Operations Inc. — FEI 3000206435

The FDA completed an inspection of Isomedix Operations Inc. on Jan 11, 2019 in Temecula, CA. 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
Jan 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Temecula, CA (United States)

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