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FDA Inspection 727297 — Frontida BioPharm Inc

Frontida BioPharm Inc — FEI 2523348

The FDA completed an inspection of Frontida BioPharm Inc on May 20, 2011 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
May 20, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Philadelphia, PA (United States)

Facility

Other inspections at this facility

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  • 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))
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Recent compliance actions

FDA data resources