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DonorConnect

FDA Regulatory Profile

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

Latest inspection
Sep 5, 2025 · 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
Inspections6Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 5, 2025Murray, UTBiologicsNo Action Indicated (NAI)3000215350
Aug 20, 2019Murray, UTBiologicsVoluntary Action Indicated (VAI)3000215350
Jun 22, 2016Murray, UTBiologicsNo Action Indicated (NAI)3000215350
Mar 14, 2013Murray, UTBiologicsNo Action Indicated (NAI)3000215350
Mar 8, 2012Murray, UTBiologicsVoluntary Action Indicated (VAI)3000215350
Oct 26, 2009Murray, UTBiologicsNo Action Indicated (NAI)3000215350

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 3000215350Murray, UT6Sep 5, 2025

FDA data resources

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