FDA Inspection 563332 — Henry Hudson, M.D.

Henry Hudson, M.D. — FEI 3007370773

The FDA completed an inspection of Henry Hudson, M.D. on Jan 30, 2009 in Tucson, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tucson, AZ (United States)

Additional Details

Clinical Investigator (CI)