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•United States

ARUP Laboratories, Inc., Salt Lake City, UT – FDA Inspections

Inspection records and compliance data for ARUP Laboratories, Inc. in Salt Lake City, Utah. 9 FDA inspections on record (1 OAI), 3 Form 483s, last inspected December 17, 2025.

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Company Profile

This profile covers ARUP Laboratories, Inc. based in Salt Lake City, Utah, United States.

FDA Inspection History

FDA inspections
9
OAI
1
VAI
1
NAI
6
Unclassified
1
Form 483s
3
Warning letters
0

First inspected July 28, 2009. Last inspected December 17, 2025.

Most cited issue areas

  • Design control - no procedures1 inspection
  • Donation interval1 inspection
  • Lack of or inadequate DHR procedures1 inspection

FDA inspections (9)

DateResultFDA center(s)Insp. #
December 17, 2025OAIMedical Devices & Rad Health · Product Evaluation: Medical Devices1295758
December 4, 2025NAIBiologics · Blood and Blood Products1294066
March 11, 2019NAIBiologics · Blood and Blood Products1086864
July 14, 2017Not classifiedHuman Drugs1036656
November 18, 2016VAIBiologics · Blood and Blood Products998801
January 30, 2015NAIBiologics · Blood and Blood Products911879
June 14, 2013NAIBiologics · Human Cellular, Tissue, and Gene Therapies836724
March 6, 2012NAIBiologics · Human Cellular, Tissue, and Gene Therapies784061
July 28, 2009NAIBiologics · Blood and Blood Products600020
FDA documents

Form 483s (1)

  • Form 483s · December 17, 2025

EIRs (1)

  • EIRs · March 11, 2019
People (1)
Matthew M. Vernon
Person
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Company Information

Name

ARUP Laboratories, Inc.

FEI Number

3004741920

Address

565 S Komas Dr, Salt Lake City, Utah 84108, United States

Country

United States

ID: 5aba7097-90ba-4744-a156-5354d35b65f7

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