FDA Inspection 1112304 — Susheel K. Kodali, M.D.

Susheel K. Kodali, M.D. — FEI 3009978491

The FDA completed an inspection of Susheel K. Kodali, M.D. on November 20, 2019 in New York, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 20, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New York, NY (United States)

Additional Details

Clinical Investigator (CI)