# FDA Inspection 1051187 - Spineguard, Sa - March 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/spineguard-sa/b83d7d8e-a55a-4b14-9bf2-3f833b2e166a
Source feed: FDA_Inspections

> FDA Inspection 1051187 for Spineguard, Sa on March 29, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051187
- Company Name: Spineguard, Sa
- Inspection Date: 2018-03-29
- 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/spineguard-sa/60aa7cf1-f580-49e7-8ebf-5c234554de68

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