FDA Inspection 890065 — Siemens Medical Solutions USA Inc

Siemens Medical Solutions USA Inc — FEI 3006814109

The FDA completed an inspection of Siemens Medical Solutions USA Inc on July 25, 2014 in Buffalo Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 25, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Buffalo Grove, IL (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures