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FDA Inspection
•Cipla Limited•November 13, 2024

Cipla Limited – FDA Inspection, Nov 13, 2024

Record Details

This FDA Inspection record concerns Cipla Limited, with an inspection on November 13, 2024, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Cipla Limited
Inspection Date
November 13, 2024
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Guerlain Ulysse (FDA Associated Person)
  • Kellia N. Hicks (FDA Associated Person)
  • Lawrence R. Deyton (FDA Associated Person)
  • Shelby N. Turner (Investigator)
View Company Profile

ID · 951ba987-ff08-4cf0-a68e-c3e82cccd492

Inspection Facts

Inspection number
1254500
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Cipla Limited

6
DateClassificationOfficeProject area
January 31, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 19, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 5, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 25, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 28, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Cipla Limited
  • FDA Inspection 1160347 - 2020-01-31
  • FDA Inspection 1099619 - 2019-07-19
  • FDA Inspection 1009388 - 2017-04-05
  • FDA Inspection 891868 - 2014-07-25
  • FDA Inspection 790473 - 2012-06-28

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