FDA Inspection 681573 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 3007282753

The FDA completed an inspection of Smith & Nephew, Inc. on September 13, 2010 in Memphis, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 13, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)