# FDA Inspection 1039353 - Pantheon Spinal LLC - January 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/pantheon-spinal-llc/94c5c5a0-d2e9-4a14-b7a8-5d34662bca7f
Source feed: FDA_Inspections

> FDA Inspection 1039353 for Pantheon Spinal LLC on January 25, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039353
- Company Name: Pantheon Spinal LLC
- Inspection Date: 2018-01-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1257008 - 2024-12-11](https://www.globalkeysolutions.net/records/fda_inspections/pantheon-spinal-llc/82081692-33f9-49f2-bf39-0828d766469b)
- [FDA Inspection 1039353 - 2018-01-25](https://www.globalkeysolutions.net/records/fda_inspections/pantheon-spinal-llc/2794bf7a-bf7f-4962-97c1-1e1381f042b3)

Company: https://www.globalkeysolutions.net/companies/pantheon-spinal-llc/4609472f-5160-483e-aa9c-1a126e039179

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