FDA Inspection 1165941 — Vein360 LLC
The FDA completed an inspection of Vein360 LLC on Feb 22, 2022 in Blue Ash, OH. 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
- Feb 22, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Blue Ash, OH (United States)