# FDA Inspection 1064567 - Epix Orthopaedics - August 07, 2018

Source: https://www.keypedia.com/records/fda_inspections/epix-orthopaedics/5eaeec8d-e23c-4eaf-81d5-405199b8874d
Source feed: FDA_Inspections

> FDA Inspection 1064567 for Epix Orthopaedics on August 07, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064567
- Company Name: Epix Orthopaedics
- Inspection Date: 2018-08-07
- 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 1064567 - 2018-08-07](https://www.keypedia.com/records/fda_inspections/epix-orthopaedics/f35a1677-8ced-4951-a2cc-726d326a861c)

Company: https://www.keypedia.com/companies/epix-orthopaedics/77db24a7-81db-42fa-a548-f093fafe854f

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