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FDA Inspection
•Cdymax (India) Pharma Private Limited•May 17, 2019

Cdymax (India) Pharma Private Limited – FDA Inspection, May 17, 2019

Record Details

This FDA Inspection record concerns Cdymax (India) Pharma Private Limited, with an inspection on May 17, 2019, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Cdymax (India) Pharma Private Limited
Inspection Date
May 17, 2019
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Gam S. Zamil (Company Rep)
View Company Profile

ID · af0d07d5-0d83-4b81-886c-3d7911eee80b

Inspection Facts

Inspection number
1093684
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Cdymax (India) Pharma Private Limited

3
DateClassificationOfficeProject area
April 25, 2025OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 31, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 14, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Cdymax (India) Pharma Private Limited
  • FDA Inspection 1271325 - 2025-04-25
  • FDA Inspection 1118683 - 2020-01-31
  • FDA Inspection 940635 - 2015-08-14

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