FDA Inspection 724339 — Kenneth A. Pettine, MD

Kenneth A. Pettine, MD — FEI 3007386776

The FDA completed an inspection of Kenneth A. Pettine, MD on May 2, 2011 in Johnstown, CO. 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
May 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Johnstown, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations