# FDA Inspection 1080822 - FUSION ORTHOPEDICS USA - December 21, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/fusion-orthopedics-usa/3bce6b3a-9355-4ad4-92b4-f76820420654
Source feed: FDA_Inspections

> FDA Inspection 1080822 for FUSION ORTHOPEDICS USA on December 21, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080822
- Company Name: FUSION ORTHOPEDICS USA
- Inspection Date: 2018-12-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1080822 - 2018-12-21](https://www.globalkeysolutions.net/records/fda_inspections/fusion-orthopedics-usa/e7e1b0a6-5814-4efd-b34a-3a92b6f7492d)

Company: https://www.globalkeysolutions.net/companies/fusion-orthopedics-usa/b7c96d15-2f2f-4f22-a225-8a76b934faf2

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