# Biomet, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/biomet-inc/ca22677e-55e1-4eeb-a8a2-beabeef1c3ad

> Inspection records and compliance data for Biomet, Inc. in Warsaw, Indiana. Access full analysis and detailed observations.

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## Details

- Name: Biomet, Inc.
- FEI Number: 1825034
- City: Warsaw
- State: Indiana
- Country Name: United States
- Address Line 1: 56 E Bell Dr
- Zip Code: 46582
- Facility Type: Medical Device

## Related Documents

- [483 - Biomet, Inc. - 2023-11-09](https://www.keypedia.com/records/483/biomet-inc/f9ffe056-57aa-4873-ab11-bf7a5b33aceb) — source: FDA, date: November 9, 2023
- [FDA Inspection 1223219 - Biomet, Inc. - 2023-11-09](https://www.keypedia.com/records/fda_inspections/biomet-inc/c45343e0-ecaa-457f-adf9-5359fac0cb14) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 9, 2023
- [483 - Biomet, Inc. - 2020-01-30](https://www.keypedia.com/records/483/biomet-inc/b32d67d4-c5a1-4e72-922e-008892846767) — source: FDA, date: January 30, 2020
- [FDA Inspection 1116404 - Biomet, Inc. - 2020-01-30](https://www.keypedia.com/records/fda_inspections/biomet-inc/72869b27-66a3-4815-b57f-9879c610ff46) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 30, 2020
- [FDA Inspection 1116404 - Biomet, Inc. - 2020-01-30](https://www.keypedia.com/records/fda_inspections/biomet-inc/3556c72e-0379-4304-9c2d-113b1108c27f) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2020
- [483 - Biomet, Inc. - 2018-04-24](https://www.keypedia.com/records/483/biomet-inc/f7299370-0bcf-4150-a52c-646f311b7c61) — source: FDA, date: April 24, 2018
- [483 - Biomet, Inc. - 2018-04-24](https://www.keypedia.com/records/483/biomet-inc/4316d727-9808-4868-8a70-c78a4b850a55) — source: FDA, date: April 24, 2018
- [FDA Inspection 1050097 - Biomet, Inc. - 2018-04-24](https://www.keypedia.com/records/fda_inspections/biomet-inc/2d994f56-3d3b-4ec8-9d48-3adf391ba04f) — classification: Official Action Indicated (OAI), source: FDA, date: April 24, 2018
- [FDA Inspection 1050097 - Biomet, Inc. - 2018-04-24](https://www.keypedia.com/records/fda_inspections/biomet-inc/3144a4fe-7541-43f9-9a01-41aa5c4522f6) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2018
- [483 - Biomet, Inc. - 2017-10-16](https://www.keypedia.com/records/483/biomet-inc/1d5dda7f-de97-40ba-b321-1dc174809dfc) — source: FDA, date: October 16, 2017
- [483_RESPONSE - Biomet, Inc. - 2016-11-22](https://www.keypedia.com/records/483_response/biomet-inc/159e464e-90ad-4ff9-a4d7-e4c8086af1be) — source: FDA, date: November 22, 2016
- [483 - Biomet, Inc. - 2016-11-22](https://www.keypedia.com/records/483/biomet-inc/67bb09d3-3d24-4e59-98e2-2f005eea6d78) — source: FDA, date: November 22, 2016
- [FDA Inspection 998381 - Biomet, Inc. - 2016-11-22](https://www.keypedia.com/records/fda_inspections/biomet-inc/e13b0a86-e21c-4b58-a7a4-14f7552987ec) — classification: Official Action Indicated (OAI), source: FDA, date: November 22, 2016
- [FDA Inspection 998381 - Biomet, Inc. - 2016-11-22](https://www.keypedia.com/records/fda_inspections/biomet-inc/4a281d67-31f4-41c9-b115-35c7cc6b7d00) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2016
- [FDA Inspection 885336 - Biomet, Inc. - 2014-06-30](https://www.keypedia.com/records/fda_inspections/biomet-inc/e208e1f5-ed81-428f-b70f-811f0d670bc4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2014
- [FDA Inspection 885336 - Biomet, Inc. - 2014-06-30](https://www.keypedia.com/records/fda_inspections/biomet-inc/8150f901-b96d-4c2a-a3cd-944d20c2ee6c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2014
- [FDA Inspection 885336 - Biomet, Inc. - 2014-06-30](https://www.keypedia.com/records/fda_inspections/biomet-inc/1ef257af-4094-4c13-b427-ab5b3c6d06e1) — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2014
- [483 - Biomet, Inc. - 2008-07-15](https://www.keypedia.com/records/483/biomet-inc/901c3c73-b66f-4268-b218-66633d64978b) — source: FDA, date: July 15, 2008

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