FDA Inspection 1112333 — Chandan B. Mehta, MD

Chandan B. Mehta, MD — FEI 3015773242

The FDA completed an inspection of Chandan B. Mehta, MD on November 21, 2019 in Detroit, MI. 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
November 21, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Detroit, MI (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations
701221 CFR 812.100Investigator lack of control of investigational devices