# FDA Inspection 1226836 - Vein360 LLC - January 08, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/vein360-llc/df0f7cda-e8e0-4513-9691-3e3d6c9072f9
Source feed: FDA_Inspections

> FDA Inspection 1226836 for Vein360 LLC on January 08, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226836
- Company Name: Vein360 LLC
- Inspection Date: 2024-01-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1165941 - 2022-02-22](https://www.globalkeysolutions.net/records/fda_inspections/vein360-llc/227e5298-8c38-4230-88bc-27abc5abae6d)
- [FDA Inspection 1165941 - 2022-02-22](https://www.globalkeysolutions.net/records/fda_inspections/vein360-llc/59af6e46-6d1d-4fc5-a2d2-ab0361608d41)

Company: https://www.globalkeysolutions.net/companies/vein360-llc/78a08449-e63e-4448-87fa-671a6885de2f

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7