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FDA Inspection 638744 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 2432235

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on November 24, 2009 in Tarrytown, NY. 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
November 24, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tarrytown, NY (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

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Recent compliance actions

FDA data resources