FDA Inspection 1015367 — Jonathan V Wright MD

Jonathan V Wright MD — FEI 3013359825

The FDA completed an inspection of Jonathan V Wright MD on June 20, 2017 in Tukwila, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tukwila, WA (United States)

Additional Details

Clinical Investigator (CI)