FDA Inspection 948368 — DDC Technologies, Inc.

DDC Technologies, Inc. — FEI 3002757272

The FDA completed an inspection of DDC Technologies, Inc. on November 9, 2015 in Oceanside, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 9, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Oceanside, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints