LifeServe Blood Center

FDA Regulatory Profile

LifeServe Blood Center has 0 FDA recalls, 82 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 29, 2026 · 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
Inspections82Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 29, 2026Ankeny, IABiologicsNo Action Indicated (NAI)3018921483
Jun 16, 2026Mitchell, SDBiologicsNo Action Indicated (NAI)3006192368
Apr 14, 2026Sioux City, IABiologicsNo Action Indicated (NAI)3011389677
Dec 18, 2025Ames, IABiologicsNo Action Indicated (NAI)3005929852
Dec 5, 2025Davenport, IABiologicsNo Action Indicated (NAI)3034208102
Dec 3, 2025Urbandale, IABiologicsNo Action Indicated (NAI)3000209837
Sep 3, 2025Marshalltown, IABiologicsNo Action Indicated (NAI)3003294564
Jul 22, 2025Aberdeen, SDBiologicsNo Action Indicated (NAI)3022881402
Jun 25, 2025Mason City, IABiologicsNo Action Indicated (NAI)3003602379
Mar 3, 2025Yankton, SDBiologicsNo Action Indicated (NAI)3025325016
Nov 22, 2024Johnston, IABiologicsNo Action Indicated (NAI)1970355
Jun 14, 2024Pella, IABiologicsNo Action Indicated (NAI)3022888869
May 24, 2024Yankton, SDBiologicsNo Action Indicated (NAI)3025325016
Apr 25, 2024Cedar Falls, IABiologicsNo Action Indicated (NAI)3004039507
Apr 11, 2024Fort Dodge, IABiologicsNo Action Indicated (NAI)3005668390
Mar 20, 2024Sioux City, IABiologicsNo Action Indicated (NAI)1970344
Dec 7, 2023Omaha, NEBiologicsNo Action Indicated (NAI)3010698750
Apr 26, 2023Mason City, IABiologicsNo Action Indicated (NAI)3003602379
Apr 19, 2023Marshalltown, IABiologicsNo Action Indicated (NAI)3003294564
Feb 1, 2023Sioux City, IABiologicsNo Action Indicated (NAI)3011389677

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 3018921483Ankeny, IA2Sep 29, 2026
FEI 3006192368Mitchell, SD7Jun 16, 2026
FEI 3011389677Sioux City, IA5Apr 14, 2026
FEI 3005929852Ames, IA8Dec 18, 2025
FEI 3034208102Davenport, IA1Dec 5, 2025
FEI 3000209837Urbandale, IA7Dec 3, 2025
FEI 3003294564Marshalltown, IA8Sep 3, 2025
FEI 3022881402Aberdeen, SD1Jul 22, 2025
FEI 3003602379Mason City, IA7Jun 25, 2025
FEI 3025325016Yankton, SD2Mar 3, 2025
FEI 1970355Johnston, IA11Nov 22, 2024
FEI 3022888869Pella, IA1Jun 14, 2024
FEI 3004039507Cedar Falls, IA6Apr 25, 2024
FEI 3005668390Fort Dodge, IA7Apr 11, 2024
FEI 1970344Sioux City, IA5Mar 20, 2024
FEI 3010698750Omaha, NE4Dec 7, 2023

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