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FDA Inspection 1096686 — Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc. — FEI 1034973

The FDA completed an inspection of Siemens Medical Solutions USA, Inc. on June 7, 2019 in Knoxville, TN. 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
June 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Knoxville, TN (United States)

Facility

Other inspections at this facility

  • 877264 (NAI Fri May 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 738774 (NAI Wed Aug 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 547060 (OAI Fri Oct 31 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources