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FDA Inspection
•Jubilant Generics Limited•March 13, 2015

Jubilant Generics Limited – FDA Inspection, Mar 13, 2015

Record Details

This FDA Inspection record concerns Jubilant Generics Limited, with an inspection on March 13, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jubilant Generics Limited
Inspection Date
March 13, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · c05248f9-18d0-422b-9979-52beaae66cd1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
921700
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Jubilant Generics Limited

9
DateClassificationOfficeProject area
August 1, 2025OAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
February 2, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 1, 2022OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 12, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 6, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Jubilant Generics Limited
  • FDA Inspection 1278253 - 2025-08-01
  • FDA Inspection 1231774 - 2024-02-02
  • FDA Inspection 1175958 - 2022-08-01
  • FDA Inspection 1137148 - 2021-03-12
  • FDA Inspection 1112459 - 2019-11-06

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