# FDA Inspection 1192014 - Kitron AB - November 10, 2022

Source: https://www.keypedia.com/records/fda_inspections/kitron-ab/4bdd1d62-60c8-4c28-af86-f5ee91c60a86
Source feed: FDA_Inspections

> FDA Inspection 1192014 for Kitron AB on November 10, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1192014
- Company Name: Kitron AB
- Inspection Date: 2022-11-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1074723 - 2018-12-13](https://www.keypedia.com/records/fda_inspections/kitron-ab/50982007-241d-4747-9f3f-3a11454737e4)

Company: https://www.keypedia.com/companies/kitron-ab/647d205a-5fcf-4f53-990f-473be4f4c4c2

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