# FDA Inspection 1210401 - BrainScope Company, Inc. - July 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/brainscope-company-inc/a42ab84f-7f2b-4a45-af77-28cbd8371012
Source feed: FDA_Inspections

> FDA Inspection 1210401 for BrainScope Company, Inc. on July 13, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210401
- Company Name: BrainScope Company, Inc.
- Inspection Date: 2023-07-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1210401 - 2023-07-13](https://www.keypedia.com/records/fda_inspections/brainscope-company-inc/a4977986-fcad-4faf-932f-232d2f8c7207)
- [FDA Inspection 1170474 - 2022-05-16](https://www.keypedia.com/records/fda_inspections/brainscope-company-inc/3eae7e0b-64df-4244-a88a-e118dce3ee79)

Company: https://www.keypedia.com/companies/brainscope-company-inc/1767d7fa-b9cf-4ad2-8096-f3ca1f24ee8b

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