FDA Inspection 1279390 — Liquid Vapor Lounge

Liquid Vapor Lounge — FEI 3011148327

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.