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FDA Inspection
•Kansas City Oncology Program IRB•March 15, 2018

Kansas City Oncology Program IRB – FDA Inspection, Mar 15, 2018

Record Details

This FDA Inspection record concerns Kansas City Oncology Program IRB, with an inspection on March 15, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Kansas City Oncology Program IRB
Inspection Date
March 15, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Carmen Y. Fisher (FDA Associated Person)
View Company Profile

ID · e8b3303f-6973-4037-99cc-06b394230d0c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1044348
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 56.115(a)(2)Minutes of IRB meetings

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kansas City Oncology Program IRB

1
DateClassificationOfficeProject area
January 26, 2012VAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Kansas City Oncology Program IRB
  • FDA Inspection 765489 - 2012-01-26

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