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CoreRX Inc.

FDA Regulatory Profile

CoreRX Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 26, 2026 · 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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 26, 2026Clearwater, FLDrugsVoluntary Action Indicated (VAI)3007209985
Mar 20, 2025Clearwater, FLBiologicsVoluntary Action Indicated (VAI)3007209985
Aug 13, 2021Clearwater, FLDrugsNo Action Indicated (NAI)3007209985
Mar 6, 2020Clearwater, FLDrugsVoluntary Action Indicated (VAI)3007209985
Sep 27, 2017Clearwater, FLDrugsVoluntary Action Indicated (VAI)3007209985
Jun 19, 2015Clearwater, FLDrugsVoluntary Action Indicated (VAI)3007209985

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 3007209985Clearwater, FL6Feb 26, 2026

FDA data resources

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