FDA Inspection 948179 — Advanced Sterilization Products

Advanced Sterilization Products — FEI 3003662624

The FDA completed an inspection of Advanced Sterilization Products on Oct 28, 2015 in Irvine, 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
Oct 28, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

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