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FDA Inspection
•Corden Pharma Chenove•February 14, 2025

Corden Pharma Chenove – FDA Inspection, Feb 14, 2025

Record Details

This FDA Inspection record concerns Corden Pharma Chenove, with an inspection on February 14, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Corden Pharma Chenove
Inspection Date
February 14, 2025
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA V. MillarW (Issuing Officer)
View Company Profile

ID · fa6d810f-d196-4589-bf3f-3c38b6e0a732

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1277830
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Corden Pharma Chenove

4
DateClassificationOfficeProject area
September 13, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 26, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 14, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 20, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Corden Pharma Chenove
  • FDA Inspection 1101908 - 2019-09-13
  • FDA Inspection 988106 - 2016-08-26
  • FDA Inspection 874552 - 2014-03-14
  • FDA Inspection 633571 - 2009-11-20

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