663938

Siemens Healthcare Diagnostics Inc — FEI 3002637618

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Norwood, MA (United States)

Citations

IDCFRDescription
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
73221 CFR 803.50(a)(2)Individual Report of Malfunction