FDA Inspection 1123885 — JOYETECH USA INC.
The FDA completed an inspection of JOYETECH USA INC. on Dec 13, 2019 in Costa Mesa, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Tobacco.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 13, 2019
- Fiscal Year
- 2020
- Product Type
- Tobacco
- Project Area
- Tobacco Post-Market Activities
- Location
- Costa Mesa, CA (United States)