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FDA Inspection
•Wayne State University Institutional Review Board•May 12, 2017

Wayne State University Institutional Review Board – FDA Inspection, May 12, 2017

Record Details

This FDA Inspection record concerns Wayne State University Institutional Review Board, with an inspection on May 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Wayne State University Institutional Review Board
Inspection Date
May 12, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Corrine M. Carter (Company Rep)
  • Neali H. Lucas (Company Rep)
View Company Profile

ID · 8c045f3b-229f-4ee9-9b38-db1d82b1ffcd

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1023236
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of Wayne State University Institutional Review Board

3
DateClassificationOfficeProject area
November 1, 2019NAICenter for Devices and Radiological HealthBioresearch Monitoring
January 26, 2012VAICenter for Devices and Radiological HealthBioresearch Monitoring
February 2, 2010OAICenter for Devices and Radiological HealthBioresearch Monitoring
Other documents for Wayne State University Institutional Review Board
  • FDA Inspection 1118237 - 2019-11-01
  • FDA Inspection 765463 - 2012-01-26
  • FDA Inspection 645453 - 2010-02-02

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