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Kentucky Blood Center Inc

FDA Regulatory Profile

Kentucky Blood Center Inc has 0 FDA recalls, 41 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 25, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections41Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 25, 2026Somerset, KYBiologicsNo Action Indicated (NAI)1048401
Jun 9, 2026Louisville, KYBiologicsNo Action Indicated (NAI)3011192341
Mar 25, 2026Louisville, KYBiologicsNo Action Indicated (NAI)3014276808
Jan 20, 2026Lexington, KYBiologicsNo Action Indicated (NAI)3007689681
Sep 22, 2025Lexington, KYBiologicsVoluntary Action Indicated (VAI)1070402
Jun 25, 2025Pikeville, KYBiologicsNo Action Indicated (NAI)1000220419
Apr 16, 2024Corbin, KYBiologicsNo Action Indicated (NAI)3022934680
Jan 25, 2024Frankfort, KYBiologicsNo Action Indicated (NAI)3023199756
Sep 18, 2023Lexington, KYBiologicsVoluntary Action Indicated (VAI)1070402
Jul 24, 2023Pikeville, KYBiologicsNo Action Indicated (NAI)1000220419
Feb 17, 2023Louisville, KYBiologicsNo Action Indicated (NAI)3014276808
Nov 17, 2022Somerset, KYBiologicsNo Action Indicated (NAI)1048401
Apr 13, 2021Louisville, KYBiologicsNo Action Indicated (NAI)3011192341
Mar 9, 2021Louisville, KYBiologicsNo Action Indicated (NAI)3014276808
Feb 10, 2020Lexington, KYBiologicsNo Action Indicated (NAI)3007689681
Aug 16, 2019Lexington, KYBiologicsNo Action Indicated (NAI)1070402
Mar 27, 2019Paducah, KYBiologicsNo Action Indicated (NAI)3013450009
Feb 26, 2018Lexington, KYBiologicsNo Action Indicated (NAI)3007689681
Feb 22, 2018Pikeville, KYBiologicsNo Action Indicated (NAI)1000220419
Feb 21, 2018Somerset, KYBiologicsNo Action Indicated (NAI)1048401

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 1048401Somerset, KY7Aug 25, 2026
FEI 3011192341Louisville, KY4Jun 9, 2026
FEI 3014276808Louisville, KY3Mar 25, 2026
FEI 3007689681Lexington, KY7Jan 20, 2026
FEI 1070402Lexington, KY10Sep 22, 2025
FEI 1000220419Pikeville, KY7Jun 25, 2025
FEI 3022934680Corbin, KY1Apr 16, 2024
FEI 3023199756Frankfort, KY1Jan 25, 2024
FEI 3013450009Paducah, KY1Mar 27, 2019

FDA data resources

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