FDA Inspection 1063861 — WCG IRB, Inc

WCG IRB, Inc — FEI 3021685

The FDA completed an inspection of WCG IRB, Inc on Aug 24, 2018 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 24, 2018
Fiscal Year
2018
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