# FDA Inspection 928000 - SPINEVISION INC - May 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/spinevision-inc/7103bbd9-3a20-4fa7-9022-59f85f206fc1
Source feed: FDA_Inspections

> FDA Inspection 928000 for SPINEVISION INC on May 19, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 928000
- Company Name: SPINEVISION INC
- Inspection Date: 2015-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/spinevision-inc/78d918da-c8cc-44e3-8bbe-1e61056cbf78

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