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Eagle Pharma Outsourcing LLC

FDA Regulatory Profile

Eagle Pharma Outsourcing LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 27, 2025 · VAI

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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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 27, 2025Hoover, ALDrugsVoluntary Action Indicated (VAI)3011688532
Aug 12, 2021Hoover, ALDrugsVoluntary Action Indicated (VAI)3011688532
May 18, 2018Hoover, ALDrugsOfficial Action Indicated (OAI)3011688532
Aug 21, 2015Hoover, ALDrugsOfficial Action Indicated (OAI)3011688532

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 3011688532Hoover, AL4Feb 27, 2025

FDA data resources

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