FDA Inspection 1019785 — Daheng New Epoch Technology, Inc.

Daheng New Epoch Technology, Inc. — FEI 3008705657

The FDA completed an inspection of Daheng New Epoch Technology, Inc. on July 14, 2017 in Beijing. 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
July 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Beijing (China)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures