# FDA Inspection 989763 - ArthroCare Corp - September 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/arthrocare-corp/44cd7ae4-9bb9-47a0-875d-2fefc88cdd74
Source feed: FDA_Inspections

> FDA Inspection 989763 for ArthroCare Corp on September 02, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989763
- Company Name: ArthroCare Corp
- Inspection Date: 2016-09-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989763 - 2016-09-02](https://www.keypedia.com/records/fda_inspections/arthrocare-corp/a7aadba6-709a-4534-bb39-2578cb7bd857)
- [FDA Inspection 840435 - 2013-07-16](https://www.keypedia.com/records/fda_inspections/arthrocare-corp/adbad710-cdfe-4a1a-96a7-7e65bd6a7da5)
- [FDA Inspection 563391 - 2009-01-30](https://www.keypedia.com/records/fda_inspections/arthrocare-corp/6909272d-c79b-481b-99ee-16b9357b85df)
- [FDA Inspection 563391 - 2009-01-30](https://www.keypedia.com/records/fda_inspections/arthrocare-corp/e6f608f4-be97-4309-8c26-52e2cea6a48e)

Company: https://www.keypedia.com/companies/arthrocare-corp/e3a31457-28fc-4410-82eb-3773d9730b27

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