# FDA Inspection 926039 - SpineForm LLC - April 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/spineform-llc/135ad49e-9087-4618-9baa-41eea427a49f
Source feed: FDA_Inspections

> FDA Inspection 926039 for SpineForm LLC on April 30, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926039
- Company Name: SpineForm LLC
- Inspection Date: 2015-04-30
- 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/spineform-llc/add55d9e-1f93-4e50-b6c8-2840194d7184

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