FDA Inspection 989881 - Somerset Medical Center IRB - September 30, 2016

FDA Inspection 989881 for Somerset Medical Center IRB on September 30, 2016. Classification: Official Action Indicated (OAI).

View on Dashboard

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 Inspection 989881 for Somerset Medical Center IRB on September 30, 2016. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 56.107(e)

21 CFR 56.108(a)(1)

21 CFR 56.108(c)

21 CFR 56.115(a)(1)

21 CFR 56.115(a)(2)

21 CFR 56.115(a)(3)

21 CFR 56.115(a)(5)

21 CFR 56.115(b)

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

Somerset Medical Center IRB

Inspection Date

September 30, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 671499a9-0c32-4097-9a90-29076a87a050

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