FDA Inspection 862502 — Matthew W. Doust, MD

Matthew W. Doust, MD — FEI 3010593279

The FDA completed an inspection of Matthew W. Doust, MD on Jan 15, 2014 in Phoenix, AZ. 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). Product area: Devices.