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FDA Inspection
•Integris Baptist Medical Center IRB•March 4, 2016

Integris Baptist Medical Center IRB – FDA Inspection, Mar 4, 2016

Record Details

This FDA Inspection record concerns Integris Baptist Medical Center IRB, with an inspection on March 4, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Integris Baptist Medical Center IRB
Inspection Date
March 4, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ccf2ad92-ed9b-4d04-bc15-987efc9389a9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
961043
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

2
  1. 21 CFR 56.104(c)Emergency use and IRB approval
  2. 21 CFR 56.108(a)(1)Initial and continuing reviews

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Integris Baptist Medical Center IRB

1
DateClassificationOfficeProject area
December 21, 2022NAIBioresearch Monitoring
Other documents for Integris Baptist Medical Center IRB
  • FDA Inspection 1193918 - 2022-12-21

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