FDA Inspection 754491 — WCG IRB, Inc

WCG IRB, Inc — FEI 3021685

The FDA completed an inspection of WCG IRB, Inc on Nov 9, 2011 in Puyallup, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 9, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Puyallup, WA (United States)

Additional Details

IRB

Citations

IDCFRDescription
720921 CFR 50.25(a)(1)Procedures, identification of those which were experimental
728121 CFR 56.108(a)(1)Initial and continuing reviews