# FDA Inspection 706941 - Seacost Biomet - January 25, 2011

Source: https://www.keypedia.com/records/fda_inspections/seacost-biomet/80ebfd98-a226-4c0a-b9d0-7791d82833de
Source feed: FDA_Inspections

> FDA Inspection 706941 for Seacost Biomet on January 25, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 706941
- Company Name: Seacost Biomet
- Inspection Date: 2011-01-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 706941 - 2011-01-25](https://www.keypedia.com/records/fda_inspections/seacost-biomet/ed26ffbc-bd54-44cf-b0fc-2b1f6d55c3ec)

Company: https://www.keypedia.com/companies/seacost-biomet/c00212a6-e3a9-41d0-98b9-a9ac4bafce33

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