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FDA Inspection
•Viyash Life Sciences Private Limited•April 25, 2025

Viyash Life Sciences Private Limited – FDA Inspection, Apr 25, 2025

Record Details

This FDA Inspection record concerns Viyash Life Sciences Private Limited, with an inspection on April 25, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Viyash Life Sciences Private Limited
Inspection Date
April 25, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Erik W. Koester (FDA Associated Person)
View Company Profile

ID · f136df12-cdb3-48e9-8c16-820bff6de350

Inspection Facts

Inspection number
1268018
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Viyash Life Sciences Private Limited

4
DateClassificationOfficeProject area
October 16, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 16, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 17, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 6, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Viyash Life Sciences Private Limited
  • FDA Inspection 1135094 - 2018-10-16
  • FDA Inspection 1042056 - 2017-11-16
  • FDA Inspection 938027 - 2015-07-17
  • FDA Inspection 771481 - 2012-03-06

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