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FDA Inspection 562346 — Implant Direct Sybron Manufacturing LLC

Implant Direct Sybron Manufacturing LLC — FEI 3001617766

The FDA completed an inspection of Implant Direct Sybron Manufacturing LLC on January 27, 2009 in Westlake Village, CA. 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 27, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Westlake Village, CA (United States)

Facility

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FDA data resources