708589

Defibtech, LLC — FEI 3003521780

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 8, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Guilford, CT (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures