# FDA Inspection 1095111 - Neurolign USA, Llc - July 02, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/neurolign-usa-llc/34ddbbad-a88c-4dc1-a556-97f927ab8166
Source feed: FDA_Inspections

> FDA Inspection 1095111 for Neurolign USA, Llc on July 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095111
- Company Name: Neurolign USA, Llc
- Inspection Date: 2019-07-02
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/neurolign-usa-llc/53c20675-c3fd-49f6-b135-907b154e5e47

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