FDA Inspection 1155885 — Smith & Nephew Inc.

Smith & Nephew Inc. — FEI 3003604053

The FDA completed an inspection of Smith & Nephew Inc. on October 26, 2021 in Andover, 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
October 26, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Andover, MA (United States)