# ClearPoint Neuro, Inc. – FDA Inspection, Jul 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/clearpoint-neuro-inc/99fd4796-7906-4dc5-9af6-3bebf0dd365d
Source feed: FDA_Inspections

> FDA inspection 1060878 of ClearPoint Neuro, Inc., July 25, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 895130 - 2014-09-10

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

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

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