# Siemens AG/Siemens Healthcare GmbH – FDA Inspection, Jan 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/6aa0e8cc-8e13-453e-8cb3-43c247be1f82
Source feed: FDA_Inspections

> FDA inspection 1196666 of Siemens AG/Siemens Healthcare GmbH, January 26, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1196666
- Company Name: Siemens AG/Siemens Healthcare GmbH
- Inspection Date: 2023-01-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1054153 - 2018-01-12](https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/b9c4c0d0-c7a7-4bb0-9aeb-b9a1a031a81c)
- FDA Inspection 979352 - 2016-07-19
- FDA Inspection 894799 - 2014-04-03
- FDA Inspection 721737 - 2011-03-03

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/siemens-agsiemens-healthcare-gmbh/8ae334de-d423-4a84-a8bd-cc3c3224c0af

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