FDA Inspection 840018 — K. Rajender Reddy

K. Rajender Reddy — FEI 3010192240

The FDA completed an inspection of K. Rajender Reddy on June 14, 2013 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 14, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Philadelphia, PA (United States)

Additional Details

Clinical Investigator (CI)