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FDA Inspection
•Siemens Medical Solutions USA, Inc.•December 12, 2014

Siemens Medical Solutions USA, Inc. – FDA Inspection, Dec 12, 2014

Record Details

This FDA Inspection record concerns Siemens Medical Solutions USA, Inc., with an inspection on December 12, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Siemens Medical Solutions USA, Inc.
Inspection Date
December 12, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 88f4afc8-7dc9-474b-a34f-508f1e8f57e5

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
907597
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 812.150(b)(8)Sponsor report of use without informed consent

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Siemens Medical Solutions USA, Inc.

6
DateClassificationOfficeProject area
August 27, 2026Not classifiedSeattle District OfficeCompliance: Devices
January 31, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 6, 2023VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 4, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
July 27, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 6 other inspections on the company page
Other documents for Siemens Medical Solutions USA, Inc.
  • FDA Inspection 1325694 - 2026-08-27
  • FDA Inspection 1228210 - 2024-01-31
  • FDA Inspection 1194297 - 2023-01-06
  • FDA Inspection 883159 - 2014-06-04
  • FDA Inspection 792025 - 2012-07-27

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