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FDA Inspection 557929 — Ivoclar Vivadent Manufacturing, Inc.

Ivoclar Vivadent Manufacturing, Inc. — FEI 2244842

The FDA completed an inspection of Ivoclar Vivadent Manufacturing, Inc. on January 21, 2009 in Somerset, NJ. 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
January 21, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Somerset, NJ (United States)

Facility

Other inspections at this facility

  • 1025860 (VAI Wed Sep 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 754045 (NAI Tue Nov 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources