# FDA Inspection 1102760 - Siemens Medical Solutions USA Inc - September 18, 2019

Source: https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/51922c53-da08-4850-98dd-8018a59ded19
Source feed: FDA_Inspections

> FDA Inspection 1102760 for Siemens Medical Solutions USA Inc on September 18, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102760
- Company Name: Siemens Medical Solutions USA Inc
- Inspection Date: 2019-09-18
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 890065 - 2014-07-25](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/d08c34a4-7a44-4ab8-ba6c-d31bed82555d)
- [FDA Inspection 890065 - 2014-07-25](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/e0e7b573-e83a-4402-b984-ce18d70603a2)
- [FDA Inspection 547938 - 2008-11-20](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/b608f828-712f-42e4-989e-ab7b97aca50b)

Company: https://www.keypedia.com/companies/siemens-medical-solutions-usa-inc/9f5eddc3-7fc9-4d09-bb45-bc5b225ca583

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