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FDA Inspection
•Kumar Organic Products Ltd.•February 8, 2019

Kumar Organic Products Ltd. – FDA Inspection, Feb 8, 2019

Record Details

This FDA Inspection record concerns Kumar Organic Products Ltd., with an inspection on February 8, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Kumar Organic Products Ltd.
Inspection Date
February 8, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Marcus A. Ray (FDA Associated Person)
View Company Profile

ID · 1cdbcdc7-c004-4688-a430-ad8289c483df

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1079870
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Kumar Organic Products Ltd.

4
DateClassificationOfficeProject area
June 13, 2025Not classifiedOffice of Inspections and Investigations
May 13, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 18, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 17, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Kumar Organic Products Ltd.
  • FDA Inspection 1276811 - 2025-06-13
  • FDA Inspection 974558 - 2016-05-13
  • FDA Inspection 890841 - 2014-07-18
  • FDA Inspection 725183 - 2011-03-17

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