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FDA Inspection 1083832 — Synthes (USA) Products LLC

Synthes (USA) Products LLC — FEI 3008812560

The FDA completed an inspection of Synthes (USA) Products LLC on September 25, 2017 in West Chester, PA. 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
September 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, PA (United States)

Facility

Other inspections at this facility

  • 1029323 (VAI Fri Oct 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032557 (NAI Tue Oct 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1028729 (VAI Fri Oct 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 695834 (NAI Fri Oct 29 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 583439 (VAI Mon Apr 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources