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FDA Inspection
•Dr. Reddy's Laboratories (EU) Ltd.•September 15, 2017

Dr. Reddy's Laboratories (EU) Ltd. – FDA Inspection, Sep 15, 2017

Record Details

This FDA Inspection record concerns Dr. Reddy's Laboratories (EU) Ltd., with an inspection on September 15, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Dr. Reddy's Laboratories (EU) Ltd.
Inspection Date
September 15, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Doan N. Singh (Issuing Officer)
View Company Profile

ID · 07c47bed-0fe6-4a48-b30b-6711df81135b

Inspection Facts

Inspection number
1036322
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Dr. Reddy's Laboratories (EU) Ltd.

3
DateClassificationOfficeProject area
September 5, 2025Not classifiedOffice of Inspections and Investigations
October 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 20, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Dr. Reddy's Laboratories (EU) Ltd.
  • FDA Inspection 1287532 - 2025-09-05
  • FDA Inspection 1119807 - 2019-10-24
  • FDA Inspection 866234 - 2013-12-20

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