# FDA Inspection 853020 - Arthrex Gmbh - September 27, 2013

Source: https://www.keypedia.com/records/fda_inspections/arthrex-gmbh/51f5c1f4-fea7-4e96-b366-eb9de394e0f7
Source feed: FDA_Inspections

> FDA Inspection 853020 for Arthrex Gmbh on September 27, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853020
- Company Name: Arthrex Gmbh
- Inspection Date: 2013-09-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 853020 - 2013-09-27](https://www.keypedia.com/records/fda_inspections/arthrex-gmbh/e3ee8a79-efc2-4ff2-be4e-a3f33412072f)

Company: https://www.keypedia.com/companies/arthrex-gmbh/efb315ef-4d91-48f2-a6a1-0848853befb7

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