Implant Direct Sybron Manufacturing LLC

Form 483FOIA Uncovered

Westlake Village, California, United StatesFEI 3001617766Issued December 02, 2019

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3001617766.

Observations5

Issue DateDecember 02, 2019

StatusNo Warning Letter

Related Inspections8

Establishment Details

Firm: Implant Direct Sybron Manufacturing LLC
Location: Westlake Village, California, United States
FEI Number: 3001617766
Product Type: Devices
Issue Date: December 02, 2019
Country: United States

Inspection History, 2009 to 2025

NAI6

VAI1

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Implant Direct Sybron Manufacturing LLC FDA Form 483, Westlake Village, California, December 2, 2019