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FDA Inspection
•Siemens Medical Solutions USA, Inc.•January 31, 2024

Siemens Medical Solutions USA, Inc. – FDA Inspection, Jan 31, 2024

Record Details

This FDA Inspection record concerns Siemens Medical Solutions USA, Inc., with an inspection on January 31, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Siemens Medical Solutions USA, Inc.
Inspection Date
January 31, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Eric C. Fox (Investigator)
View Company Profile

ID · e432435b-7d09-4d81-9c67-9ea5019ebc58

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1228210
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 820.198(a)Lack of or inadequate complaint procedures

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 6, 2023VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 12, 2014VAICenter for Devices and Radiological HealthBioresearch Monitoring
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 1194297 - 2023-01-06
  • FDA Inspection 907597 - 2014-12-12
  • FDA Inspection 883159 - 2014-06-04
  • FDA Inspection 792025 - 2012-07-27

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