# Arthrex, Inc. – FDA Inspection, Oct 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/arthrex-inc/3527512d-3639-4b9c-a245-804da80662e4
Source feed: FDA_Inspections

> FDA inspection 1051363 of Arthrex, Inc., October 20, 2017. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051363
- Company Name: Arthrex, Inc.
- Inspection Date: 2017-10-20
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Florida District Office
- Citation Count: 0

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- [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