# FDA Inspection 817735 - Ossur Americas, Inc. - February 08, 2013

Source: https://www.keypedia.com/records/fda_inspections/ossur-americas-inc/c8ced0e0-e9e9-45ec-b661-7cb81c88594a
Source feed: FDA_Inspections

> FDA Inspection 817735 for Ossur Americas, Inc. on February 08, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817735
- Company Name: Ossur Americas, Inc.
- Inspection Date: 2013-02-08
- 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 904376 - 2014-11-21](https://www.keypedia.com/records/fda_inspections/ossur-americas-inc/14c89545-d981-4800-bc41-f86c3c30b7f1)
- [FDA Inspection 817735 - 2013-02-08](https://www.keypedia.com/records/fda_inspections/ossur-americas-inc/5167063b-bab3-4ab2-bd4b-73783e83c6ee)

Company: https://www.keypedia.com/companies/ossur-americas-inc/027e41ab-91a6-4602-815f-b2086c774f69

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