FDA Inspection 1181293 — Resonance Technology Inc

Resonance Technology Inc — FEI 1000306474

The FDA completed an inspection of Resonance Technology Inc on Oct 6, 2022 in Northridge, 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 6, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Northridge, CA (United States)

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