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FDA Inspection
•Amneal Pharmaceuticals Inc.•January 18, 2018

Amneal Pharmaceuticals Inc. – FDA Inspection, Jan 18, 2018

Record Details

This FDA Inspection record concerns Amneal Pharmaceuticals Inc., with an inspection on January 18, 2018, issued by the New York District Office, covering human drugs.

Company
Amneal Pharmaceuticals Inc.
Inspection Date
January 18, 2018
Product Type
Human Drugs
Office
New York District Office
Person
  • Robert C. Horan (FDA Associated Person)
View Company Profile

ID · e5316bf2-c323-448f-983f-cfdec3406fd5

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1037898
FDA center
Human Drugs
Project area
Generic Drug Evaluation
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

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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