FDA Inspection 1325632 — Karthik V. Giridhar, MD

Karthik V. Giridhar, MD — FEI 3043421414

The FDA completed an inspection of Karthik V. Giridhar, MD on Jun 18, 2026 in Rochester, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.