# FDA Inspection 821770 - Arthrocare Corporation - March 01, 2013

Source: https://www.keypedia.com/records/fda_inspections/arthrocare-corporation/3a74a859-ceb4-4f9a-aabe-fe1b1122f621
Source feed: FDA_Inspections

> FDA Inspection 821770 for Arthrocare Corporation on March 01, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821770
- Company Name: Arthrocare Corporation
- Inspection Date: 2013-03-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 821770 - 2013-03-01](https://www.keypedia.com/records/fda_inspections/arthrocare-corporation/2d27a759-8fd4-4793-8fb1-f145d7d61027)
- [FDA Inspection 723758 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/arthrocare-corporation/a1c2b366-ada3-411d-8f2b-f02cd0175c6f)
- [FDA Inspection 723758 - 2011-04-21](https://www.keypedia.com/records/fda_inspections/arthrocare-corporation/05bbf532-0857-44e0-a020-7c77ec2373f8)

Company: https://www.keypedia.com/companies/arthrocare-corporation/ba662545-9e49-4ab6-a2eb-a0f1b4a21de5

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