FDA EIR - Advarra IRB - May 27, 2021

FDA EIR for Advarra IRB on May 27, 2021. Product: Devices. Access full analysis and detailed observations.

One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.

Record Summary

FDA EIR for Advarra IRB on May 27, 2021. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 50.51

FD&C Act 520(g)

21 CFR 50.24(a)(7)

FD&C Act 505(i)

21 CFR 50

21 CFR 809.10(c)

21 CFR 50.24(a)(3)

21 CFR 50.20

21 CFR 50.24(a)(6)

21 CFR 812.2

Get More Insights

Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.

1.5M+ regulatory data points

Real-time compliance monitoring

Interactive analytics dashboard

Looking for more records? Our platform provides access to thousands of similar regulatory documents with advanced search and filtering capabilities.

Record Information

Company

Advarra IRB

Inspection Date

May 27, 2021

Product Type

Devices

Office

Center for Devices and Radiological Health

People

ID: b6fe5d28-e806-4300-b924-8da21434490a

View on Dashboard

Transform Regulatory Data into Actionable Intelligence

Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.

Try KeyPedia Today

Explore our real use cases and discover our features in depth.

Subscribe to our newsletter

Get the latest updates and insights delivered to your inbox