FDA Inspection 981507 — Sonendo Inc

Sonendo Inc — FEI 3010817521

The FDA completed an inspection of Sonendo Inc on Feb 26, 2016 in Laguna Hills, 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
Feb 26, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Laguna Hills, CA (United States)