1064813

CareFusion 303, Inc. — FEI 2016493

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 6, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
317221 CFR 820.198(c)Investigation of device failures