FDA Inspection 606405 — Smith & Nephew Inc

Smith & Nephew Inc — FEI 3005551626

The FDA completed an inspection of Smith & Nephew Inc on Aug 19, 2009 in Memphis, TN. 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
Aug 19, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)