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FDA Inspection 1199981 — Smith & Nephew Orthopaedics GmbH

Smith & Nephew Orthopaedics GmbH — FEI 3002465897

The FDA completed an inspection of Smith & Nephew Orthopaedics GmbH on January 12, 2023 in Tuttlingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 12, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)

Facility

Other inspections at this facility

  • 1045278 (NAI Thu Feb 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022654 (NAI Thu Apr 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928966 (NAI Thu May 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 823996 (NAI Fri Feb 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 681881 (OAI Thu Jul 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources