FDA Inspection 1123885 — JOYETECH USA INC.

JOYETECH USA INC. — FEI 3013278729

The FDA completed an inspection of JOYETECH USA INC. on December 13, 2019 in Costa Mesa, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Tobacco.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2019
Fiscal Year
2020
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Costa Mesa, CA (United States)