FDA Inspection 1215918 — Rajendra R. Makkar, MD

Rajendra R. Makkar, MD — FEI 3009801867

The FDA completed an inspection of Rajendra R. Makkar, MD on August 15, 2023 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
August 15, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Los Angeles, CA (United States)

Additional Details

Clinical Investigator (CI)