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FDA Inspection
•Cohance Lifesciences Limited•February 15, 2018

Cohance Lifesciences Limited – FDA Inspection, Feb 15, 2018

Record Details

This FDA Inspection record concerns Cohance Lifesciences Limited, with an inspection on February 15, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Cohance Lifesciences Limited
Inspection Date
February 15, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • June P. Page (FDA Associated Person)
View Company Profile

ID · c3fdedea-4c22-4b83-a805-2135836e7f2e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1041216
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Cohance Lifesciences Limited

7
DateClassificationOfficeProject area
August 5, 2026Not classifiedOffice of Inspections and Investigations
February 23, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 1, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 14, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 8, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Cohance Lifesciences Limited
  • FDA Inspection 1335432 - 2026-08-05
  • FDA Inspection 1234405 - 2024-02-23
  • FDA Inspection 1110488 - 2019-11-01
  • FDA Inspection 973825 - 2016-04-14
  • FDA Inspection 854615 - 2013-02-08

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