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FDA Inspection
•Amneal Pharmaceuticals Pvt. Ltd.•April 12, 2017

Amneal Pharmaceuticals Pvt. Ltd. – FDA Inspection, Apr 12, 2017

Record Details

This FDA Inspection record concerns Amneal Pharmaceuticals Pvt. Ltd., with an inspection on April 12, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Amneal Pharmaceuticals Pvt. Ltd.
Inspection Date
April 12, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Yumi J. Hiramine (Issuing Officer)
View Company Profile

ID · c21b7ee4-ebdf-44ba-b1ff-965433eddc25

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1011379
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Amneal Pharmaceuticals Pvt. Ltd.

7
DateClassificationOfficeProject area
July 14, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 21, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 24, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 22, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Amneal Pharmaceuticals Pvt. Ltd.
  • FDA Inspection 1216256 - 2023-07-14
  • FDA Inspection 1121776 - 2020-02-21
  • FDA Inspection 1091111 - 2019-05-24
  • FDA Inspection 1067930 - 2018-08-24
  • FDA Inspection 1031432 - 2017-09-22

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