# FDA Inspection 1014280 - NeuroLogica Corporation - June 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/neurologica-corporation/52d3040f-b6f5-4861-9171-604c9003fa3f
Source feed: FDA_Inspections

> FDA Inspection 1014280 for NeuroLogica Corporation on June 15, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014280
- Company Name: NeuroLogica Corporation
- Inspection Date: 2017-06-15
- 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/neurologica-corporation/112b8be4-8d99-4b9b-b6f8-0335d0ba9af0

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