# Arthrex, Inc. – FDA Inspection, Nov 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/arthrex-inc/026fb82f-14a3-4eb4-9bba-28de8b04a0d8
Source feed: FDA_Inspections

> FDA inspection 1101957 of Arthrex, Inc., November 30, 2018. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101957
- Company Name: Arthrex, Inc.
- Inspection Date: 2018-11-30
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Florida District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1256990 - 2025-01-13](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c1ab486b-3e07-429a-9db2-0a4512da02dc)
- [FDA Inspection 1206181 - 2023-05-05](https://www.keypedia.com/records/fda_inspections/arthrex-inc/db41feaf-cb3c-46d0-8676-c2fc59ce221b)
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- [FDA Inspection 984081 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/arthrex-inc/c8a55436-e787-4a35-8a73-f6ce301c51d3)
- FDA Inspection 624886 - 2009-10-30

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

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9
