800358

InVitroCare, Inc — FEI 3004882774

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Frederick, MD (United States)

Citations

IDCFRDescription
342621 CFR 820.50(a)(1)Documented evaluation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures