FDA Inspection 1041637 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 1020279

The FDA completed an inspection of Smith & Nephew, Inc. on Feb 2, 2018 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
Feb 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Memphis, TN (United States)

Additional details

Postmarket Audit Inspections

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