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FDA Inspection 585525 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 2517506

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on May 8, 2009 in Newark, DE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 8, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Newark, DE (United States)

Facility

Other inspections at this facility

  • 875518 (VAI Wed Apr 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 813459 (NAI Mon Dec 17 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768876 (OAI Thu Feb 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources