# FDA Inspection 1208820 - Sonesta Medical AB - June 07, 2023

Source: https://www.keypedia.com/records/fda_inspections/sonesta-medical-ab/52ceec9e-d765-4135-9344-873d0c3ab44c
Source feed: FDA_Inspections

> FDA Inspection 1208820 for Sonesta Medical AB on June 07, 2023. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208820
- Company Name: Sonesta Medical AB
- Inspection Date: 2023-06-07
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208820 - 2023-06-07](https://www.keypedia.com/records/fda_inspections/sonesta-medical-ab/2f76c162-981e-4153-8b34-4b5e4e822fc9)
- [FDA Inspection 1014756 - 2017-06-14](https://www.keypedia.com/records/fda_inspections/sonesta-medical-ab/2cd391dd-dd36-4cf0-928b-fd79064a5373)
- [FDA Inspection 1014756 - 2017-06-14](https://www.keypedia.com/records/fda_inspections/sonesta-medical-ab/488e87fe-745b-4522-bcca-1748de6ef13f)

Company: https://www.keypedia.com/companies/sonesta-medical-ab/76fa77cf-7355-453a-a882-167e416b48a2

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