FDA Inspection 1107470 — Neelakantan Anand, MD

Neelakantan Anand, MD — FEI 3015533953

The FDA completed an inspection of Neelakantan Anand, MD on October 24, 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.