FDA Inspection 709912 — Anson M Cheung MD

Anson M Cheung MD — FEI 3008759499

The FDA completed an inspection of Anson M Cheung MD on February 11, 2011 in Vancouver. 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
February 11, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Vancouver (Canada)

Additional Details

Clinical Investigator (CI)