FDA Inspection 996812 — Fulton D'Souza, MD

Fulton D'Souza, MD — FEI 3012763843

The FDA completed an inspection of Fulton D'Souza, MD on Nov 16, 2016 in Bangalore. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 16, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Bangalore (India)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.