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FDA Inspection 821920 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 1219913

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on February 20, 2013 in East Walpole, MA. 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
February 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
East Walpole, MA (United States)

Facility

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  • 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))
  • 754929 (OAI Wed Jan 04 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources