FDA Inspection 788180 — Taylor, Dr Robert W

Taylor, Dr Robert W — FEI 3009616460

The FDA completed an inspection of Taylor, Dr Robert W on June 22, 2012 in Saint Louis, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450821 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations