# FDA Inspection 1100117 - NEOTERYX, LLC - August 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/neoteryx-llc/09c8ba8a-b459-46e9-a573-40052d6b0b7e
Source feed: FDA_Inspections

> FDA Inspection 1100117 for NEOTERYX, LLC on August 15, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100117
- Company Name: NEOTERYX, LLC
- Inspection Date: 2019-08-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/neoteryx-llc/9d4da458-4998-4bb7-9136-035cc26b8f43

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