FDA Inspection 898652 — Siemens Healthcare Diagnostics Inc.

Siemens Healthcare Diagnostics Inc. — FEI 3002755490

The FDA completed an inspection of Siemens Healthcare Diagnostics Inc. on October 2, 2014 in Brookfield, CT. 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
October 2, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Brookfield, CT (United States)