FDA Inspection 810604 — Rajendra R. Makkar, MD

Rajendra R. Makkar, MD — FEI 3009801867

The FDA completed an inspection of Rajendra R. Makkar, MD on December 14, 2012 in Los Angeles, CA. 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
December 14, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Los Angeles, CA (United States)

Additional Details

Clinical Investigator (CI)