# FDA Inspection 1020990 - Orthoaccel Technologies, Inc - February 17, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/orthoaccel-technologies-inc/ffd9dbda-fec1-4fec-bf6c-a9dae1a2f612/
Source feed: FDA_Inspections

> FDA Inspection 1020990 for Orthoaccel Technologies, Inc on February 17, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1020990
- Company Name: Orthoaccel Technologies, Inc
- Inspection Date: 2017-02-17
- 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 1020990 - 2017-02-17](https://www.globalkeysolutions.net/api/records/fda_inspections/orthoaccel-technologies-inc/e3570dbb-1a32-4f19-b4dd-c1d89454ee28/)

Company: https://www.globalkeysolutions.net/companies/orthoaccel-technologies-inc/904d490a-62d6-4a2d-b16f-b4dffd6cd494

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