FDA Inspection 998962 — Dr. Savita Rangarajan

Dr. Savita Rangarajan — FEI 3012862727

The FDA completed an inspection of Dr. Savita Rangarajan on Nov 28, 2016 in London. 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 28, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
London (United Kingdom)

Additional Details

Clinical Investigator (CI)

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