# Siemens Medical Solutions USA, Inc. – FDA Inspection, Mar 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/66e3492e-2c6e-4842-b3e7-2a3bc2104e80
Source feed: FDA_Inspections

> FDA inspection 916426 of Siemens Medical Solutions USA, Inc., March 27, 2015. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803, 806 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916426
- Company Name: Siemens Medical Solutions USA, Inc.
- Inspection Date: 2015-03-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1022705 - 2017-04-06](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/6617c149-ba26-469e-9b41-2d9dabea144b)
- [FDA Inspection 976280 - 2016-04-15](https://www.keypedia.com/records/fda_inspections/siemens-medical-solutions-usa-inc/af234197-0a3d-40af-8d78-657f3a781312)
- FDA Inspection 839435 - 2013-07-10
- FDA Inspection 759664 - 2011-12-19

Company: https://www.keypedia.com/companies/siemens-medical-solutions-usa-inc/beb8a4fa-57e8-4950-8fb2-2dec7b75a09e

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