FDA Inspection 569059 — DePuy Spine, Inc.

DePuy Spine, Inc. — FEI 1526439

The FDA completed an inspection of DePuy Spine, Inc. on March 11, 2009 in Raynham, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 11, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Raynham, MA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
292821 CFR 812.40Sponsors' general responsibilities
294921 CFR 812.46(a)Sponsor securing investigator compliance
304921 CFR 812.150(b)(5)Sponsor progress reports for significant risk study