FDA Inspection 784218 — Kevin Waltz, OD, MD

Kevin Waltz, OD, MD — FEI 3009453953

The FDA completed an inspection of Kevin Waltz, OD, MD on May 23, 2012 in Indianapolis, IN. 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.