FDA Inspection 767936 — Joseph Mills MD

Joseph Mills MD — FEI 3009327348

The FDA completed an inspection of Joseph Mills MD on February 9, 2012 in Houston, TX. 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
February 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Houston, TX (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
298121 CFR 812.140(a)(2)(i)Investigator device accountability inadequate