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FDA Inspection
•Amneal Pharmaceuticals Inc.•July 10, 2018

Amneal Pharmaceuticals Inc. – FDA Inspection, Jul 10, 2018

Record Details

This FDA Inspection record concerns Amneal Pharmaceuticals Inc., with an inspection on July 10, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Amneal Pharmaceuticals Inc.
Inspection Date
July 10, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Karen L. Kosar (FDA Associated Person)
  • Peter S. Diak (Issuing Officer)
  • Tara K. Carmody (FDA Associated Person)
View Company Profile

ID · 2704b680-9f95-4854-8ed5-328212f590ab

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1065634
FDA center
Human Drugs
Project area
Bioresearch Monitoring

Other FDA inspections of Amneal Pharmaceuticals Inc.

15
DateClassificationOfficeProject area
September 25, 2026Not classifiedNew York District Office
August 28, 2026Not classifiedNew York District Office
June 7, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 20, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 18, 2019NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 15 other inspections on the company page
Other documents for Amneal Pharmaceuticals Inc.
  • FDA Inspection 1305048 - 2026-09-25
  • FDA Inspection 1286562 - 2026-08-28
  • FDA Inspection 1207398 - 2023-06-07
  • FDA Inspection 1116040 - 2019-12-20
  • FDA Inspection 1089916 - 2019-04-18

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