FDA Inspection 1114048 — Abreast Technology Inc

Abreast Technology Inc — FEI 3006943033

The FDA completed an inspection of Abreast Technology Inc on December 27, 2019 in Vernon, CA. 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: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 27, 2019
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Vernon, CA (United States)

Additional Details

FSVP

Citations

IDCFRDescription
1825421 CFR 1.502(a)Develop FSVP