FDA Inspection 1097351 — Vertigo Vapor Inc
The FDA completed an inspection of Vertigo Vapor Inc on March 19, 2019 in Henderson, NV. 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
- March 19, 2019
- Fiscal Year
- 2019
- Product Type
- Tobacco
- Project Area
- Tobacco Post-Market Activities
- Location
- Henderson, NV (United States)