FDA Inspection 722279 — William Beaumont Hospital IRB

William Beaumont Hospital IRB — FEI 1823222

The FDA completed an inspection of William Beaumont Hospital IRB on May 4, 2011 in Royal Oak, MI. 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
May 4, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Royal Oak, MI (United States)

Additional Details

IRB

Citations

IDCFRDescription
728121 CFR 56.108(a)(1)Initial and continuing reviews
731821 CFR 56.115(a)(2)Minutes of IRB meetings