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FDA Inspection
•Dr. Sandeep Kumar Gupta•August 31, 2018

Dr. Sandeep Kumar Gupta – FDA Inspection, Aug 31, 2018

Record Details

This FDA Inspection record concerns Dr. Sandeep Kumar Gupta, with an inspection on August 31, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Dr. Sandeep Kumar Gupta
Inspection Date
August 31, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Kent A. Conforti (Company Rep)
View Company Profile

ID · e16d29df-c338-41de-84bf-5b08661c5877

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1071165
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

Other FDA inspections of Dr. Sandeep Kumar Gupta

1
DateClassificationOfficeProject area
January 18, 2012VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Dr. Sandeep Kumar Gupta
  • FDA Inspection 766447 - 2012-01-18

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