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FDA Inspection 581756 — Synthes, Inc.

Synthes, Inc. — FEI 3005180112

The FDA completed an inspection of Synthes, Inc. on April 27, 2009 in West Chester, PA. 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
April 27, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
West Chester, PA (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 859106 (VAI Wed Nov 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 831886 (NAI Thu May 16 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 806156 (VAI Fri Oct 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 732622 (OAI Thu Sep 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 620039 (NAI Thu Oct 08 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources