FDA Inspection 700982 — Smith & Nephew Inc

Smith & Nephew Inc — FEI 3005551626

The FDA completed an inspection of Smith & Nephew Inc on Dec 2, 2010 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
Dec 2, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)