FDA Inspection 1147814 — K. Rajender Reddy

K. Rajender Reddy — FEI 3010192240

The FDA completed an inspection of K. Rajender Reddy on July 28, 2021 in Philadelphia, PA. 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
July 28, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Philadelphia, PA (United States)

Additional Details

Clinical Investigator (CI)