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

Source: https://www.keypedia.com/companies/arl-biopharma-inc/358f0af9-fe47-4cd8-b43e-a4b9eacf1b21

> 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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## Details

- Name: ARL Biopharma, Inc.
- FEI Number: 3003644883
- Facility Type: Contract Testing Laboratory
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: 840 Research Pkwy Ste 546
- City: Oklahoma City
- State: Oklahoma
- Zip Code: 73104
- Country Name: United States
- Address: 840 Research Pkwy Ste 546, Oklahoma City, Oklahoma 73104, United States
- Country: United States

## Related Documents

- FDA Inspection 1322550 - ARL Biopharma, Inc. - 2026-05-22 — source: FDA, date: May 22, 2026
- [FDA Inspection 1102393 - ARL Biopharma, Inc. - 2019-09-20](https://www.keypedia.com/records/fda_inspections/arl-biopharma-inc/00b13fc7-baf0-4864-922b-b9359c7c19bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 20, 2019
- [483 - ARL Biopharma, Inc. - 2019-09-05](https://www.keypedia.com/records/483/arl-biopharma-inc/4e19e914-ce9d-4342-96dc-f564f8420248) — source: FDA, date: September 5, 2019
- [FDA Inspection 965921 - ARL Biopharma, Inc. - 2016-03-25](https://www.keypedia.com/records/fda_inspections/arl-biopharma-inc/d5a8ac1d-9744-43f0-a76e-6727f2380fa5) — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2016
- [483 - ARL Biopharma, Inc. - 2012-11-08](https://www.keypedia.com/records/483/arl-biopharma-inc/6ca790e1-4e13-4b6a-91b5-960aa9cd8387) — source: FDA, date: November 8, 2012
- FDA Inspection 806356 - ARL Biopharma, Inc. - 2012-11-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 8, 2012
- FDA Inspection 701726 - ARL Biopharma, Inc. - 2010-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2010
- FDA Inspection 651237 - ARL Biopharma, Inc. - 2010-02-18 — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2010

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