# FDA Inspection 1018552 - Epic Extremity, LLC - May 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/epic-extremity-llc/68ab2081-4365-4e58-b5fd-bf7cf156ec7e
Source feed: FDA_Inspections

> FDA Inspection 1018552 for Epic Extremity, LLC on May 19, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018552
- Company Name: Epic Extremity, LLC
- Inspection Date: 2017-05-19
- 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 1082406 - 2019-03-06](https://www.keypedia.com/records/fda_inspections/epic-extremity-llc/16927cd6-220e-4491-b700-990963f97c34)
- [FDA Inspection 1018552 - 2017-05-19](https://www.keypedia.com/records/fda_inspections/epic-extremity-llc/059a0c9a-ff52-47df-8914-9497f65d4634)

Company: https://www.keypedia.com/companies/epic-extremity-llc/275f37cd-3485-4111-8a90-37b7c83a3b8d

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