# FDA Inspection 1263631 - NextBeam - March 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/nextbeam/32880e87-ce31-4561-b382-98da680ea4eb
Source feed: FDA_Inspections

> FDA Inspection 1263631 for NextBeam on March 13, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263631
- Company Name: NextBeam
- Inspection Date: 2025-03-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1263631 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/nextbeam/11d5db15-7812-4534-a446-e7df5ca528ff)
- [FDA Inspection 1263631 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/nextbeam/f02481fc-b5af-4dcf-b13d-01135ae1fab3)
- [FDA Inspection 1263631 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/nextbeam/a3d4c81f-bfcb-4333-9aea-1ecf3edcc6e4)

Company: https://www.keypedia.com/companies/nextbeam/50a36300-885c-498e-ade5-5db6ef2f010f

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d