# FDA Inspection 1187539 - Siemens Medical Solutions USA, Inc - October 26, 2022

Source: https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/45dffe84-5fc8-4db6-a876-8dc3a469cd62
Source feed: FDA_Inspections

> FDA Inspection 1187539 for Siemens Medical Solutions USA, Inc on October 26, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1187539
- Company Name: Siemens Medical Solutions USA, Inc
- Inspection Date: 2022-10-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1187539 - 2022-10-26](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/c59933a2-8af9-4f27-9bd9-4b7d3b69d835)
- [FDA Inspection 902685 - 2014-11-07](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/e7b1e94f-083f-4b79-8f2a-d8c93b1b7ea2)
- [FDA Inspection 605404 - 2009-07-31](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/357b3faa-87ee-4427-a761-665624e9c28d)

Company: https://www.keypedia.com/companies/siemens-medical-solutions-usa-inc/6edd49f1-05c5-4343-a2b7-4008bb315702

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