# Arthrex, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/arthrex-inc/e18abb8a-3bf8-462d-b279-f969cd710c14

> Inspection records and compliance data for Arthrex, Inc. in Naples, Florida. Access full analysis and detailed observations.

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## Details

- Name: Arthrex, Inc.
- FEI Number: 1220246
- City: Naples
- State: Florida
- Country Name: United States
- Address Line 1: 1370 Creekside Blvd
- Zip Code: 34108

## Related Documents

- [483 - Arthrex, Inc. - 2025-01-13](https://www.keypedia.com/records/483/arthrex-inc/14aa3216-f2de-4704-9684-27c19ae5bbae) — source: FDA, date: January 13, 2025
- [FDA Inspection 1256990 - Arthrex, Inc. - 2025-01-13](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c1ab486b-3e07-429a-9db2-0a4512da02dc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2025
- [FDA Inspection 1256990 - Arthrex, Inc. - 2025-01-13](https://www.keypedia.com/records/fda_inspections/arthrex-inc/07abdf4d-2fb6-4fde-914d-39f6d9cd6c51) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2025
- [483 - Arthrex, Inc. - 2023-05-05](https://www.keypedia.com/records/483/arthrex-inc/a4c87741-bc0e-439d-b521-920db2e08c6f) — source: FDA, date: May 5, 2023
- [FDA Inspection 1206181 - Arthrex, Inc. - 2023-05-05](https://www.keypedia.com/records/fda_inspections/arthrex-inc/db41feaf-cb3c-46d0-8676-c2fc59ce221b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 5, 2023
- [FDA Inspection 1206181 - Arthrex, Inc. - 2023-05-05](https://www.keypedia.com/records/fda_inspections/arthrex-inc/84399818-3db6-4312-85c7-53a31ae5e1ff) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 5, 2023
- [EIR - Arthrex, Inc. - 2016-08-25](https://www.keypedia.com/records/eir/arthrex-inc/cb34c4d8-e56c-4016-9c5a-dd1062bae1f5) — source: FDA, date: August 25, 2016
- [FDA Inspection 984081 - Arthrex, Inc. - 2016-08-25](https://www.keypedia.com/records/fda_inspections/arthrex-inc/b6873f18-9cbc-4440-954b-1a550f6f9bd0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 25, 2016
- [FDA Inspection 984081 - Arthrex, Inc. - 2016-08-25](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c8a55436-e787-4a35-8a73-f6ce301c51d3) — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2016
- [EIR - Arthrex, Inc. - 2009-10-30](https://www.keypedia.com/records/eir/arthrex-inc/516e4bae-d8e1-4d29-ac0d-598b368c9795) — source: FDA, date: October 30, 2009
- [FDA Inspection 624886 - Arthrex, Inc. - 2009-10-30](https://www.keypedia.com/records/fda_inspections/arthrex-inc/83f6c982-47e5-461f-8389-d0db8c210185) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2009
- [FDA Inspection 624886 - Arthrex, Inc. - 2009-10-30](https://www.keypedia.com/records/fda_inspections/arthrex-inc/7adbbe40-ad8f-43d6-b4d7-c7ed8c0b4fc6) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2009
- [FDA Inspection 621663 - Arthrex, Inc. - 2009-10-09](https://www.keypedia.com/records/fda_inspections/arthrex-inc/69b01e82-4598-4d2f-9f4b-284f2dbb8b4d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 9, 2009

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