# FDA Inspection 1208700 - NeuroField, Inc. - June 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/neurofield-inc/577fa8c3-e05e-474c-919e-a3ac3964cf12
Source feed: FDA_Inspections

> FDA Inspection 1208700 for NeuroField, Inc. on June 23, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208700
- Company Name: NeuroField, Inc.
- Inspection Date: 2023-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/neurofield-inc/f654f932-8d5b-4c42-8e3d-362b06ef27bd

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