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FDA Inspection 1276700 — Implant Direct Sybron Manufacturing LLC

Implant Direct Sybron Manufacturing LLC — FEI 3001617766

The FDA completed an inspection of Implant Direct Sybron Manufacturing LLC on July 24, 2025 in Westlake Village, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 24, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Westlake Village, CA (United States)

Facility

Other inspections at this facility

  • 1141791 (VAI Wed May 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111746 (OAI Mon Dec 02 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923088 (NAI Tue Apr 21 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 872940 (NAI Thu Apr 03 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768936 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources