623870

Kem Medical Products Corp — FEI 2432141

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 27, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hauppauge, NY (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures