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

Source: https://www.globalkeysolutions.net/records/fda_inspections/linxens-sweden-ab/5d04811d-63d2-4bfb-ac9d-42855cd5b7a1
Source feed: FDA_Inspections

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

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## 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: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1253832 - 2024-11-07](https://www.globalkeysolutions.net/records/fda_inspections/linxens-sweden-ab/7d74af6a-c79e-482a-aeb4-e166c2ed32db)

Company: https://www.globalkeysolutions.net/companies/linxens-sweden-ab/1b13d3be-7e73-446a-b435-cf569fea1e43

Office: https://www.globalkeysolutions.net/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8