FDA Inspection 1279390 — Liquid Vapor Lounge

Liquid Vapor Lounge — FEI 3011148327

The FDA completed an inspection of Liquid Vapor Lounge on August 12, 2025 in Oklahoma City, OK. 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
August 12, 2025
Fiscal Year
2025
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Oklahoma City, OK (United States)