FDA Inspection 1073960 — Khosla, Sundeep, MD

Khosla, Sundeep, MD — FEI 3014866650

The FDA completed an inspection of Khosla, Sundeep, MD on Dec 7, 2018 in Rochester, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.