# FDA Inspection 853087 - ARTHREX GMBH - September 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/arthrex-gmbh/491e644e-dd74-4735-a92f-c6fc720239a8
Source feed: FDA_Inspections

> FDA Inspection 853087 for ARTHREX GMBH on September 25, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853087
- Company Name: ARTHREX GMBH
- Inspection Date: 2013-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/arthrex-gmbh/ba4604cd-08b5-41b6-803a-740fcdf59cf5

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7