878759

Acuderm, Inc. — FEI 1035236

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 9, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Ft Lauderdale, FL (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
369621 CFR 820.100(b)Documentation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation