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FDA Inspection
•Azurity Pharmaceuticals, Inc.•December 12, 2025

Azurity Pharmaceuticals, Inc. – FDA Inspection, Dec 12, 2025

Record Details

This FDA Inspection record concerns Azurity Pharmaceuticals, Inc., with an inspection on December 12, 2025, covering drugs.

Company
Azurity Pharmaceuticals, Inc.
Inspection Date
December 12, 2025
Product Type
Drugs
People
  • Armen H. Youssoufian (Issuing Officer)
  • Erik W. Koester (FDA Associated Person)
View Company Profile

ID · 7c93bd99-060c-47b1-906c-ce6cdfe7bf52

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1297348
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Azurity Pharmaceuticals, Inc.

8
DateClassificationOfficeProject area
February 19, 2025Not classifiedNew England District OfficeDrug Quality Assurance
March 2, 2023Not classifiedNew England District OfficeDrug Quality Assurance
February 24, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 26, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 20, 2017Not classifiedNew England District Office
View all 8 other inspections on the company page
Other documents for Azurity Pharmaceuticals, Inc.
  • FDA Inspection 1261303 - 2025-02-19
  • FDA Inspection 1199279 - 2023-03-02
  • FDA Inspection 1163010 - 2022-02-24
  • FDA Inspection 1100022 - 2019-07-26
  • FDA Inspection 1038444 - 2017-12-20

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