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Frontida BioPharm Inc

FDA Regulatory Profile

Frontida BioPharm Inc has 0 FDA recalls, 21 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Apr 2, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections21Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 2, 2026Philadelphia, PADrugsNo Action Indicated (NAI)2523348
Oct 24, 2025Aurora, ILDrugsVoluntary Action Indicated (VAI)3008087151
Jul 22, 2025Philadelphia, PATobaccoNo Action Indicated (NAI)2523348
Jul 22, 2025Philadelphia, PATobaccoNo Action Indicated (NAI)3004464206
Dec 7, 2023Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Feb 26, 2021Aurora, ILDrugsNo Action Indicated (NAI)3008087151
Jul 19, 2019Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Jul 20, 2017Philadelphia, PADrugsNo Action Indicated (NAI)3004464206
Mar 31, 2017Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Feb 18, 2016Aurora, ILFood/CosmeticsNo Action Indicated (NAI)3008087151
Jul 17, 2015Philadelphia, PADrugsOfficial Action Indicated (OAI)2523348
Jul 25, 2014Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Feb 26, 2013Aurora, ILDrugsNo Action Indicated (NAI)3008087151
Sep 13, 2012Philadelphia, PADrugsNo Action Indicated (NAI)3004464206
Jan 27, 2012Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Aug 16, 2011Aurora, ILDrugsNo Action Indicated (NAI)3008087151
May 20, 2011Philadelphia, PADrugsNo Action Indicated (NAI)3004464206
May 20, 2011Philadelphia, PADrugsVoluntary Action Indicated (VAI)2523348
Jan 5, 2010Aurora, ILDrugsNo Action Indicated (NAI)3008087151
Jun 30, 2009Philadelphia, PADrugsNo Action Indicated (NAI)2523348

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 2523348Philadelphia, PA11Apr 2, 2026
FEI 3008087151Aurora, IL6Oct 24, 2025
FEI 3004464206Philadelphia, PA4Jul 22, 2025

FDA data resources

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