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FDA Inspection 1102760 — Siemens Medical Solutions USA Inc

Siemens Medical Solutions USA Inc — FEI 3006814109

The FDA completed an inspection of Siemens Medical Solutions USA Inc on September 18, 2019 in Buffalo Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Buffalo Grove, IL (United States)

Facility

Other inspections at this facility

  • 890065 (NAI Fri Jul 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 547938 (NAI Thu Nov 20 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources