# FDA Inspection 806730 - Arthrosurface, Inc. - November 09, 2012

Source: https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/ae1c7f8c-0a1a-4e25-8e2a-3c228323782a
Source feed: FDA_Inspections

> FDA Inspection 806730 for Arthrosurface, Inc. on November 09, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 806730
- Company Name: Arthrosurface, Inc.
- Inspection Date: 2012-11-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1311064 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/eeb59ec8-3e04-4307-94cb-6487c401ca98)
- [FDA Inspection 1311064 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/fe34a0f9-f06a-44e5-8105-461cd6b77193)
- [FDA Inspection 1311064 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/1d343fde-a95e-4cda-a8fc-cfb3f4e1012d)
- [FDA Inspection 1311064 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/488fa9e8-70a0-40ec-915f-a1f0966fd27c)
- [FDA Inspection 1279142 - 2025-08-06](https://www.keypedia.com/records/fda_inspections/arthrosurface-inc/c9519291-61c4-4c2b-a5aa-df77513fab08)

Company: https://www.keypedia.com/companies/arthrosurface-inc/4d18e49d-3a81-498f-a2cf-63d66c4907f5

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