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ImpactLife

FDA Regulatory Profile

ImpactLife has 0 FDA recalls, 141 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 28, 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
Inspections141Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 28, 2026Coralville, IABiologicsNo Action Indicated (NAI)1000510716
Sep 23, 2026Dubuque, IABiologicsNo Action Indicated (NAI)3003960009
Aug 14, 2026Saint Peters, MOBiologicsNo Action Indicated (NAI)3009755290
Jul 7, 2026Madison, WIBiologicsNo Action Indicated (NAI)3020605119
Apr 20, 2026Macomb, ILBiologicsNo Action Indicated (NAI)3003744945
Feb 2, 2026Cedar Rapids, IABiologicsNo Action Indicated (NAI)3005692903
Jan 28, 2026Galesburg, ILBiologicsNo Action Indicated (NAI)3003319042
Jan 15, 2026Cedar Rapids, IABiologicsNo Action Indicated (NAI)3009588529
Dec 22, 2025Fairview Heights, ILBiologicsNo Action Indicated (NAI)3021602461
Nov 19, 2025Moline, ILBiologicsNo Action Indicated (NAI)1470264
Aug 28, 2025Springfield, ILBiologicsNo Action Indicated (NAI)3011078001
Jul 3, 2025Urbana, ILBiologicsVoluntary Action Indicated (VAI)1470270
May 9, 2025Monona, WIBiologicsVoluntary Action Indicated (VAI)3015522161
Feb 14, 2025Davenport, IABiologicsNo Action Indicated (NAI)1970356
Jan 24, 2025Ottumwa, IABiologicsNo Action Indicated (NAI)1970361
Oct 11, 2024Arnold, MOBiologicsNo Action Indicated (NAI)3029729833
Aug 23, 2024Earth City, MOBiologicsNo Action Indicated (NAI)3004157291
Aug 15, 2024Springfield, ILBiologicsNo Action Indicated (NAI)1470254
May 30, 2024Davenport, IABiologicsNo Action Indicated (NAI)3005754990
Apr 24, 2024Saint Louis, MOBiologicsNo Action Indicated (NAI)3005841600

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 1000510716Coralville, IA8Sep 28, 2026
FEI 3003960009Dubuque, IA8Sep 23, 2026
FEI 3009755290Saint Peters, MO5Aug 14, 2026
FEI 3020605119Madison, WI1Jul 7, 2026
FEI 3003744945Macomb, IL6Apr 20, 2026
FEI 3005692903Cedar Rapids, IA7Feb 2, 2026
FEI 3003319042Galesburg, IL6Jan 28, 2026
FEI 3009588529Cedar Rapids, IA6Jan 15, 2026
FEI 3021602461Fairview Heights, IL2Dec 22, 2025
FEI 1470264Moline, IL6Nov 19, 2025
FEI 3011078001Springfield, IL4Aug 28, 2025
FEI 1470270Urbana, IL6Jul 3, 2025
FEI 3015522161Monona, WI2May 9, 2025
FEI 1970356Davenport, IA10Feb 14, 2025
FEI 1970361Ottumwa, IA8Jan 24, 2025
FEI 3029729833Arnold, MO1Oct 11, 2024
FEI 3004157291Earth City, MO7Aug 23, 2024
FEI 1470254Springfield, IL5Aug 15, 2024
FEI 3005754990Davenport, IA8May 30, 2024
FEI 3005841600Saint Louis, MO7Apr 24, 2024
FEI 1937912Burlington, IA8Jan 30, 2024
FEI 1937802Muscatine, IA7Jan 11, 2024
FEI 3003370273Danville, IL5Aug 26, 2022
FEI 3019882186Decatur, IL1Aug 24, 2022
FEI 3000719226Mattoon, IL4Aug 22, 2022
FEI 3016435215Peoria, IL1May 11, 2022
FEI 3005752939Maryville, IL2Jun 28, 2019

FDA data resources

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