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FDA Inspection 547060 — Siemens Medical Solutions USA, Inc.

Siemens Medical Solutions USA, Inc. — FEI 1034973

The FDA completed an inspection of Siemens Medical Solutions USA, Inc. on October 31, 2008 in Knoxville, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 31, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Knoxville, TN (United States)

Facility

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  • 738774 (NAI Wed Aug 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

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