FDA Inspection 1241161 — Dunamis Medical LLC

Dunamis Medical LLC — FEI 3011061237

The FDA completed an inspection of Dunamis Medical LLC on Jun 11, 2024 in Greenville, AL. 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
Jun 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Greenville, AL (United States)