FDA Inspection 1339610 — RST-Sanexas

RST-Sanexas — FEI 3002893067

The FDA completed an inspection of RST-Sanexas on Sep 17, 2026 in Henderson, NV. 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
Sep 17, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Henderson, NV (United States)

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