FDA Inspection 955900 - Willis-Knighton Health System IRB - January 28, 2016

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Copilot

Record Details

This FDA Inspection record concerns Willis-Knighton Health System IRB, with an inspection on January 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Willis-Knighton Health System IRB
Inspection Date: January 28, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 2d7d74cb-d9fc-4f9b-97ea-708aa2bcfd93

Violation Codes4

21 CFR 56.108(a)(1)21 CFR 56.110(b)21 CFR 56.111(a)(4)21 CFR 56.115(a)(2)

Full citation text and observation details available on the Dashboard.