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FDA Inspection
•RCRC Independent Review Board (IRB) dba Salus IRB•June 7, 2024

RCRC Independent Review Board (IRB) dba Salus IRB – FDA Inspection, Jun 7, 2024

Record Details

This FDA Inspection record concerns RCRC Independent Review Board (IRB) dba Salus IRB, with an inspection on June 7, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
RCRC Independent Review Board (IRB) dba Salus IRB
Inspection Date
June 7, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Iris C. Macinnes (Issuing Officer)
  • Lan T. Tran (Investigator)
View Company Profile

ID · e60f3b60-dce2-4af2-b6ff-3d6119f0393c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1240575
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

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 RCRC Independent Review Board (IRB) dba Salus IRB

2
DateClassificationOfficeProject area
February 14, 2018NAICenter for Devices and Radiological HealthBioresearch Monitoring
October 14, 2010NAIBioresearch Monitoring
Other documents for RCRC Independent Review Board (IRB) dba Salus IRB
  • FDA Inspection 1049438 - 2018-02-14
  • FDA Inspection 695467 - 2010-10-14

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