FDA Inspection 547938 — Siemens Medical Solutions USA Inc

Siemens Medical Solutions USA Inc — FEI 3006814109

The FDA completed an inspection of Siemens Medical Solutions USA Inc on November 20, 2008 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
November 20, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo Grove, IL (United States)