Home / Inspections / 737289

FDA Inspection 737289 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 1219913

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on July 21, 2011 in East Walpole, MA. 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
July 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
East Walpole, MA (United States)

Facility

Other inspections at this facility

  • 1163970 (VAI Tue Mar 08 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043709 (VAI Fri Mar 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018565 (VAI Fri May 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 929757 (NAI Wed May 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821920 (NAI Wed Feb 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources