FDA Inspection 994815 — David A. Heimansohn, M.D.

David A. Heimansohn, M.D. — FEI 3004575642

The FDA completed an inspection of David A. Heimansohn, M.D. on November 15, 2016 in Carmel, IN. 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
November 15, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Carmel, IN (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations