752181

Kerma Medical Products, Inc — FEI 1000123280

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 4, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Suffolk, VA (United States)

Citations

IDCFRDescription
320121 CFR 820.40(a)Not approved or obsolete document retrieval
369621 CFR 820.100(b)Documentation