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FDA Inspection 681881 — Smith & Nephew Orthopaedics GmbH

Smith & Nephew Orthopaedics GmbH — FEI 3002465897

The FDA completed an inspection of Smith & Nephew Orthopaedics GmbH on July 22, 2010 in Tuttlingen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tuttlingen (Germany)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

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  • 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))

Recent compliance actions

FDA data resources