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FDA Inspection
•ARL Biopharma, Inc.•March 25, 2016

ARL Biopharma, Inc. – FDA Inspection, Mar 25, 2016

Record Details

This FDA Inspection record concerns ARL Biopharma, Inc., with an inspection on March 25, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
ARL Biopharma, Inc.
Inspection Date
March 25, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · d5a8ac1d-9744-43f0-a76e-6727f2380fa5

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
965921
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of ARL Biopharma, Inc.

5
DateClassificationOfficeProject area
May 22, 2026Not classifiedDallas District Office
September 20, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 8, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 19, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 18, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for ARL Biopharma, Inc.
  • FDA Inspection 1322550 - 2026-05-22
  • FDA Inspection 1102393 - 2019-09-20
  • FDA Inspection 806356 - 2012-11-08
  • FDA Inspection 701726 - 2010-11-19
  • FDA Inspection 651237 - 2010-02-18

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