FDA Inspection 853213 — DDC Technologies, Inc.

DDC Technologies, Inc. — FEI 3002757272

The FDA completed an inspection of DDC Technologies, Inc. on October 25, 2013 in Oceanside, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 25, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Oceanside, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
342621 CFR 820.50(a)(1)Documented evaluation
369621 CFR 820.100(b)Documentation