# FDA Inspection 1253832 - Linxens Sweden AB - November 07, 2024

Source: https://www.keypedia.com/records/fda_inspections/linxens-sweden-ab/351934a3-eabe-49e9-b3fe-ea8298aa5c7e
Source feed: FDA_Inspections

> FDA Inspection 1253832 for Linxens Sweden AB on November 07, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1253832
- Company Name: Linxens Sweden AB
- Inspection Date: 2024-11-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1253832 - 2024-11-07](https://www.keypedia.com/records/fda_inspections/linxens-sweden-ab/c70c3636-006d-45f2-8431-ea6a5427bcf8)

Company: https://www.keypedia.com/companies/linxens-sweden-ab/aba1a039-abb0-4f76-89e5-cdcbe4db976f

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