FDA Inspection 1101110 — BMF Labs

BMF Labs — FEI 3013854460

The FDA completed an inspection of BMF Labs on July 11, 2019 in Greensboro, NC. 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
July 11, 2019
Fiscal Year
2019
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Greensboro, NC (United States)