# FDA Inspection 1223661 - Techfit Digital Surgery Inc - November 10, 2023

Source: https://www.keypedia.com/records/fda_inspections/techfit-digital-surgery-inc/a15f50ff-2284-4ad9-8916-68be7997dd2e
Source feed: FDA_Inspections

> FDA Inspection 1223661 for Techfit Digital Surgery Inc on November 10, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1223661
- Company Name: Techfit Digital Surgery Inc
- Inspection Date: 2023-11-10
- 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 1223661 - 2023-11-10](https://www.keypedia.com/records/fda_inspections/techfit-digital-surgery-inc/87440fe8-d869-412a-8324-046e51f23cb9)

Company: https://www.keypedia.com/companies/techfit-digital-surgery-inc/c8800c94-7e5d-4c8a-8eac-6ea9eecf2bbd

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