820624

Endoplus — FEI 3000719482

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Mundelein, IL (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures