FDA Inspection 917095 — Jason J. Jones MD

Jason J. Jones MD — FEI 3011053541

The FDA completed an inspection of Jason J. Jones MD on January 23, 2015 in Sioux City, IA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sioux City, IA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
298121 CFR 812.140(a)(2)(i)Investigator device accountability inadequate