# FDA Inspection 1270862 - ELEKTA SOLUTIONS AB - May 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/elekta-solutions-ab/d2889637-dded-427f-a2e1-d7e447a58d05
Source feed: FDA_Inspections

> FDA Inspection 1270862 for ELEKTA SOLUTIONS AB on May 22, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1270862
- Company Name: ELEKTA SOLUTIONS AB
- Inspection Date: 2025-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1270862 - 2025-05-22](https://www.keypedia.com/records/fda_inspections/elekta-solutions-ab/a44c718e-9e6f-4358-8d40-11a9d032a3fc)
- [FDA Inspection 1270862 - 2025-05-22](https://www.keypedia.com/records/fda_inspections/elekta-solutions-ab/0eb6bd4b-7ccc-4cc9-8a0f-798301ebbcdb)
- [FDA Inspection 1270862 - 2025-05-22](https://www.keypedia.com/records/fda_inspections/elekta-solutions-ab/6800afc8-1266-46a1-90c0-aff9d16f5ffb)

Company: https://www.keypedia.com/companies/elekta-solutions-ab/e0d3ae85-8bab-4278-89b3-c50160ebc162

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