FDA Inspection 1181293 — Resonance Technology Inc

Resonance Technology Inc — FEI 1000306474

The FDA completed an inspection of Resonance Technology Inc on October 6, 2022 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 6, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)