FDA Inspection 1039378 — Dr. K.R. Raveendra

Dr. K.R. Raveendra — FEI 3013794373

The FDA completed an inspection of Dr. K.R. Raveendra on Dec 15, 2017 in Bangalore. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 15, 2017
Fiscal Year
2018
Product Type
Drugs
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.