# ELEKTA SOLUTIONS AB – FDA Inspection, May 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/elekta-solutions-ab/a44c718e-9e6f-4358-8d40-11a9d032a3fc
Source feed: FDA_Inspections

> FDA inspection 1270862 of ELEKTA SOLUTIONS AB, May 22, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 3

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

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

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