FDA Inspection 1280225 — RyMed Technologies, LLC

RyMed Technologies, LLC — FEI 3005951712

The FDA completed an inspection of RyMed Technologies, LLC on August 28, 2025 in Austin, TX. 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
August 28, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Austin, TX (United States)