# Siemens Healthcare Diagnostics, Inc. – FDA Inspection, May 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/bdc63a3b-10b2-4e3a-ac9f-d6475501f23d
Source feed: FDA_Inspections

> FDA inspection 1012263 of Siemens Healthcare Diagnostics, Inc., May 31, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012263
- Company Name: Siemens Healthcare Diagnostics, Inc.
- Inspection Date: 2017-05-31
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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- [FDA Inspection 896868 - 2014-09-19](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/dffc1307-b7f1-4368-b49e-3199709e9d38)
- FDA Inspection 827292 - 2013-03-13

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

Company: https://www.keypedia.com/companies/siemens-healthcare-diagnostics-inc/edcf8312-14f0-41fb-a21f-77f1872bdc36

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