FDA Inspection 1122514 — Abomination HQ, LLP

Abomination HQ, LLP — FEI 3013057798

The FDA completed an inspection of Abomination HQ, LLP on Dec 5, 2019 in Gulfport, MS. 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 5, 2019
Fiscal Year
2020
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Gulfport, MS (United States)

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