# Implant Direct Sybron Manufacturing LLC, Westlake Village, CA – FDA Inspections

Source: https://www.keypedia.com/companies/implant-direct-sybron-manufacturing-llc/56a57268-60f3-4c99-93ba-98bc06bf4f44

> Inspection records and compliance data for Implant Direct Sybron Manufacturing LLC in Westlake Village, California. 10 FDA inspections on record (1 OAI), last inspected July 24, 2025.

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## Details

- Name: Implant Direct Sybron Manufacturing LLC
- FEI Number: 3001617766
- Address Line 1: 3050 E Hillcrest Dr
- City: Westlake Village
- State: California
- Zip Code: 91362
- Country Name: United States
- Address: 3050 E Hillcrest Dr, Westlake Village, California 91362, United States
- Country: United States

## Related Documents

- FDA Inspection 1276700 - Implant Direct Sybron Manufacturing LLC - 2025-07-24 — source: FDA, date: July 24, 2025
- FDA Inspection 1276700 - Implant Direct Sybron Manufacturing LLC - 2025-07-24 — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2025
- [FDA Inspection 1266772 - Implant Direct Sybron Manufacturing LLC - 2025-04-02](https://www.keypedia.com/records/fda_inspections/implant-direct-sybron-manufacturing-llc/b8fd51e3-336b-48d4-9a47-f3a8bf87268d) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2025
- [483 - Implant Direct Sybron Manufacturing LLC - 2021-05-12](https://www.keypedia.com/records/483/implant-direct-sybron-manufacturing-llc/4984495c-31c6-418f-b74d-68b508e28ab9) — source: FDA, date: May 12, 2021
- FDA Inspection 1141791 - Implant Direct Sybron Manufacturing LLC - 2021-05-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2021
- FDA Inspection 1141791 - Implant Direct Sybron Manufacturing LLC - 2021-05-12 — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2021
- [483 - Implant Direct Sybron Manufacturing LLC - 2019-12-02](https://www.keypedia.com/records/483/implant-direct-sybron-manufacturing-llc/a6adc243-853e-46e4-87e2-8918671630d1) — source: FDA, date: December 2, 2019
- [FDA Inspection 1111746 - Implant Direct Sybron Manufacturing LLC - 2019-12-02](https://www.keypedia.com/records/fda_inspections/implant-direct-sybron-manufacturing-llc/10676b52-ebf1-41ee-8179-cad3c1e6a0f0) — classification: Official Action Indicated (OAI), source: FDA, date: December 2, 2019
- FDA Inspection 1060206 - Implant Direct Sybron Manufacturing LLC - 2018-03-27 — source: FDA, date: March 27, 2018
- FDA Inspection 923088 - Implant Direct Sybron Manufacturing LLC - 2015-04-21 — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2015
- FDA Inspection 872940 - Implant Direct Sybron Manufacturing LLC - 2014-04-03 — classification: No Action Indicated (NAI), source: FDA, date: April 3, 2014
- FDA Inspection 872940 - Implant Direct Sybron Manufacturing LLC - 2014-04-03 — classification: No Action Indicated (NAI), source: FDA, date: April 3, 2014

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