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Hybrid Pharma LLC

FDA Regulatory Profile

Hybrid Pharma LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Nov 9, 2023 · OAI

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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 8, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 9, 2023Deerfield Beach, FLDrugsOfficial Action Indicated (OAI)3011319445
Sep 3, 2021Deerfield Beach, FLDrugsOfficial Action Indicated (OAI)3011319445
Jun 20, 2019Deerfield Beach, FLDrugsOfficial Action Indicated (OAI)3011319445
Jul 28, 2016Deerfield Beach, FLDrugsOfficial Action Indicated (OAI)3011319445

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 3011319445Deerfield Beach, FL4Nov 9, 2023

FDA data resources

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