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FDA Inspection 982340 — Implant Direct Sybron International, LLC

Implant Direct Sybron International, LLC — FEI 3009036368

The FDA completed an inspection of Implant Direct Sybron International, LLC on June 28, 2016 in Las Vegas, NV. 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
June 28, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Las Vegas, NV (United States)

Facility

Other inspections at this facility

  • 1028754 (NAI Tue Sep 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988719 (NAI Mon Aug 29 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891481 (NAI Thu Aug 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources