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FDA Inspection 813459 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 2517506

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on December 17, 2012 in Newark, DE. 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
December 17, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newark, DE (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 875518 (VAI Wed Apr 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768876 (OAI Thu Feb 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 585525 (VAI Fri May 08 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources