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FDA Inspection 1045278 — Smith & Nephew Orthopaedics GmbH

Smith & Nephew Orthopaedics GmbH — FEI 3002465897

The FDA completed an inspection of Smith & Nephew Orthopaedics GmbH on February 8, 2018 in Tuttlingen. 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
February 8, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tuttlingen (Germany)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 1199981 (VAI Thu Jan 12 2023 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