FDA Inspection 1100271 — Magellan Technology Inc

Magellan Technology Inc — FEI 3011704622

The FDA completed an inspection of Magellan Technology Inc on Jul 24, 2019 in Buffalo, NY. 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 24, 2019
Fiscal Year
2019
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Buffalo, NY (United States)

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