# FDA Inspection 1060878 - ClearPoint Neuro, Inc. - July 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearpoint-neuro-inc/4368627c-e54d-4229-acb0-17b502c1c5e0
Source feed: FDA_Inspections

> FDA Inspection 1060878 for ClearPoint Neuro, Inc. on July 25, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060878
- Company Name: ClearPoint Neuro, Inc.
- Inspection Date: 2018-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060878 - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/clearpoint-neuro-inc/99fd4796-7906-4dc5-9af6-3bebf0dd365d)
- [FDA Inspection 895130 - 2014-09-10](https://www.globalkeysolutions.net/records/fda_inspections/clearpoint-neuro-inc/8c06cecb-e055-40fc-9650-4ec6e87c704c)

Company: https://www.globalkeysolutions.net/companies/clearpoint-neuro-inc/6d7c9cb9-14d9-4785-8538-4ca6d28f3e70

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