FDA Inspection 1298434 — Medwaves Inc

Medwaves Inc — FEI 3005382058

The FDA completed an inspection of Medwaves Inc on Dec 18, 2025 in San Diego, 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
Dec 18, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

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