FDA Inspection 1025802 — Dr. Radha Krishnan

Dr. Radha Krishnan — FEI 3013564378

The FDA completed an inspection of Dr. Radha Krishnan on August 11, 2017 in Rosebank. 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
August 11, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rosebank (United Kingdom)

Additional Details

Clinical Investigator (CI)