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•United States

ARL Biopharma, Inc., Oklahoma City, OK – FDA Inspections

Inspection records and compliance data for ARL Biopharma, Inc. in Oklahoma City, Oklahoma. 6 FDA inspections on record, 1 Form 483, last inspected May 22, 2026.

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Company Profile

This profile covers ARL Biopharma, Inc. based in Oklahoma City, Oklahoma, United States.

FDA Inspection History

FDA inspections
6
OAI
0
VAI
2
NAI
3
Unclassified
1
Form 483s
1
Warning letters
0

First inspected February 18, 2010. Last inspected May 22, 2026.

FDA inspections (6)

DateResultFDA center(s)Insp. #
May 22, 2026Not classifiedHuman Drugs1322550
September 20, 2019VAIHuman Drugs · Drug Quality Assurance1102393
March 25, 2016NAIHuman Drugs · Drug Quality Assurance965921
November 8, 2012VAIHuman Drugs · Drug Quality Assurance806356
November 19, 2010NAIHuman Drugs · Drug Quality Assurance701726
February 18, 2010NAIHuman Drugs · Drug Quality Assurance651237
FDA documents

Form 483s (2)

  • Form 483s · September 5, 2019
  • Form 483s · November 8, 2012
People (1)
Margaret M. Annes
Person
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Q LABS, LLC
Company Information

Name

ARL Biopharma, Inc.

FEI Number

3003644883

Address

840 Research Pkwy Ste 546, Oklahoma City, Oklahoma 73104, United States

Country

United States

ID: 358f0af9-fe47-4cd8-b43e-a4b9eacf1b21

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