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FDA Inspection 929757 — Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. — FEI 1219913

The FDA completed an inspection of Siemens Healthcare Diagnostics, Inc. on May 20, 2015 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
May 20, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
East Walpole, MA (United States)

Additional Details

Postmarket Audit Inspections

Facility

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  • 821920 (NAI Wed Feb 20 2013 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