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FDA Inspection 890268 — Frontida BioPharm Inc

Frontida BioPharm Inc — FEI 2523348

The FDA completed an inspection of Frontida BioPharm Inc on July 25, 2014 in Philadelphia, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 25, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Philadelphia, PA (United States)

Facility

Other inspections at this facility

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  • 1279864 (NAI Tue Jul 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1226606 (VAI Thu Dec 07 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1097023 (VAI Fri Jul 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007832 (VAI Fri Mar 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources