FDA Inspection 576507 — Richard D. Guyer, MD

Richard D. Guyer, MD — FEI 3001665786

The FDA completed an inspection of Richard D. Guyer, MD on April 7, 2009 in Plano, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.