FDA Inspection 1098769 — Rajendra R. Makkar, MD

Rajendra R. Makkar, MD — FEI 3009801867

The FDA completed an inspection of Rajendra R. Makkar, MD on August 5, 2019 in Los Angeles, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.