FDA Inspection 1015137 — Smith & Nephew, Inc.

Smith & Nephew, Inc. — FEI 1219602

The FDA completed an inspection of Smith & Nephew, Inc. on May 25, 2017 in Mansfield, MA. 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
May 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Mansfield, MA (United States)