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FDA Inspection
•Cipla Limited•August 25, 2026

Cipla Limited – FDA Inspection, Aug 25, 2026

Record Details

This FDA Inspection record concerns Cipla Limited, with an inspection on August 25, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Cipla Limited
Inspection Date
August 25, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Jeffrey P. Raimondi (Investigator)
  • Jose E. Melendez (FDA Associated Person)
  • Xiaokuang Lai (FDA Associated Person)
View Company Profile

ID · 8e984a05-d69e-4ebb-beb1-b0eca787a4ba

Inspection Facts

Inspection number
1331746
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Cipla Limited

8
DateClassificationOfficeProject area
February 17, 2023OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 13, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 23, 2017Not classifiedOffice of Inspections and InvestigationsGeneric Drug Evaluation
January 27, 2017Not classifiedOffice of Inspections and Investigations
View all 8 other inspections on the company page
Other documents for Cipla Limited
  • FDA Inspection 1198343 - 2023-02-17
  • FDA Inspection 1094880 - 2019-05-17
  • FDA Inspection 1048005 - 2018-04-13
  • FDA Inspection 1019068 - 2017-06-23
  • FDA Inspection 1007876 - 2017-01-27

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