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FDA Inspection
•University of Missouri - Columbia Research Reactor Center•August 15, 2019

University of Missouri - Columbia Research Reactor Center – FDA Inspection, Aug 15, 2019

Record Details

This FDA Inspection record concerns University of Missouri - Columbia Research Reactor Center, with an inspection on August 15, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
University of Missouri - Columbia Research Reactor Center
Inspection Date
August 15, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Jonathan G Gayechuway (Issuing Officer)
  • Peng Zhou (Investigator)
  • Simone E. Pitts (FDA Associated Person)
View Company Profile

ID · 6654cb5c-f09c-4b32-897d-3437a3076df4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1100816
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of University of Missouri - Columbia Research Reactor Center

3
DateClassificationOfficeProject area
October 23, 2025Not classifiedKansas City District Office
August 19, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 29, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for University of Missouri - Columbia Research Reactor Center
  • FDA Inspection 1289150 - 2025-10-23
  • FDA Inspection 982800 - 2016-08-19
  • FDA Inspection 808859 - 2012-11-29

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