FDA Inspection 1101110 — BMF Labs

BMF Labs — FEI 3013854460

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

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