FDA Inspection 1279102 — Kaohinani Longwolf, MD

Kaohinani Longwolf, MD — FEI 3038623204

The FDA completed an inspection of Kaohinani Longwolf, MD on August 13, 2025 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.