FDA Inspection 1287668 — Resonance Technology Inc

Resonance Technology Inc — FEI 1000306474

The FDA completed an inspection of Resonance Technology Inc on October 17, 2025 in Northridge, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 17, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Northridge, CA (United States)

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation