FDA Inspection 1039882 — Dunamis Medical LLC
The FDA completed an inspection of Dunamis Medical LLC on Nov 16, 2017 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
- Nov 16, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Greenville, AL (United States)