# FDA Inspection 1018565 - Siemens Healthcare Diagnostics, Inc. - May 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/ad654162-f57f-4806-aeb3-b8d4f94c8a12
Source feed: FDA_Inspections

> FDA Inspection 1018565 for Siemens Healthcare Diagnostics, Inc. on May 12, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018565
- Company Name: Siemens Healthcare Diagnostics, Inc.
- Inspection Date: 2017-05-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/siemens-healthcare-diagnostics-inc/2d2218be-bbbe-4685-81fc-9addbac958c7

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