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ARUP Laboratories, Inc.

FDA Regulatory Profile

ARUP Laboratories, Inc. has 0 FDA recalls, 20 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 4, 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
Inspections20Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 4, 2025Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920
Nov 6, 2024Sandy, UTBiologicsVoluntary Action Indicated (VAI)1720911
Jun 13, 2024Salt Lake City, UTBiologicsNo Action Indicated (NAI)3008974012
Aug 30, 2019Sandy, UTBiologicsNo Action Indicated (NAI)1720911
Mar 14, 2019Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3008974012
Mar 11, 2019Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920
Jan 18, 2017Sandy, UTBiologicsNo Action Indicated (NAI)1720911
Dec 2, 2016Salt Lake City, UTBiologicsNo Action Indicated (NAI)3008974012
Nov 18, 2016Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3004741920
Feb 27, 2015Sandy, UTBiologicsNo Action Indicated (NAI)1720911
Feb 13, 2015Salt Lake City, UTBiologicsNo Action Indicated (NAI)3008974012
Jan 30, 2015Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920
Jun 14, 2013Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920
Feb 22, 2013Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3008974012
Feb 15, 2013Sandy, UTBiologicsVoluntary Action Indicated (VAI)1720911
Mar 6, 2012Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920
Nov 18, 2011Salt Lake City, UTBiologicsVoluntary Action Indicated (VAI)3008974012
May 20, 2011Sandy, UTBiologicsNo Action Indicated (NAI)1720911
Sep 25, 2009Sandy, UTBiologicsNo Action Indicated (NAI)1720911
Jul 28, 2009Salt Lake City, UTBiologicsNo Action Indicated (NAI)3004741920

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 3004741920Salt Lake City, UT7Dec 4, 2025
FEI 1720911Sandy, UT7Nov 6, 2024
FEI 3008974012Salt Lake City, UT6Jun 13, 2024

FDA data resources

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