FDA Inspection 1020607 — Brijeshwar S. Maini, M.D.

Brijeshwar S. Maini, M.D. — FEI 3005660697

The FDA completed an inspection of Brijeshwar S. Maini, M.D. on June 30, 2017 in Delray Beach, FL. 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
June 30, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Delray Beach, FL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate