FDA Inspection 984209 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 1020279

The FDA completed an inspection of Smith & Nephew, Inc. on Aug 17, 2016 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 17, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)

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