FDA Inspection 1226836 — Vein360 LLC
The FDA completed an inspection of Vein360 LLC on Jan 8, 2024 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
- Jan 8, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Blue Ash, OH (United States)