FDA Inspection 839676 — Kenneth A. Pettine, MD

Kenneth A. Pettine, MD — FEI 3007386776

The FDA completed an inspection of Kenneth A. Pettine, MD on June 28, 2013 in Johnstown, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Johnstown, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
298421 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate