FDA Inspection 1279864 — Frontida BioPharm Inc

Frontida BioPharm Inc — FEI 2523348

The FDA completed an inspection of Frontida BioPharm Inc on Jul 22, 2025 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Tobacco.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 22, 2025
Fiscal Year
2025
Product Type
Tobacco
Project Area
Tobacco Post-Market Activities
Location
Philadelphia, PA (United States)

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