# FDA Inspection 1281634 - Ototronix, LLC - September 05, 2025

Source: https://www.keypedia.com/records/fda_inspections/ototronix-llc/a877354d-cfc2-4ac8-a721-7be13ddcee4d
Source feed: FDA_Inspections

> FDA Inspection 1281634 for Ototronix, LLC on September 05, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1281634
- Company Name: Ototronix, LLC
- Inspection Date: 2025-09-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1281634 - 2025-09-05](https://www.keypedia.com/records/fda_inspections/ototronix-llc/e7cba93e-8882-4253-91df-a319e13dd411)
- [FDA Inspection 1281634 - 2025-09-05](https://www.keypedia.com/records/fda_inspections/ototronix-llc/d722e63f-f628-464f-af6c-591586b197e5)
- [FDA Inspection 1020239 - 2017-07-20](https://www.keypedia.com/records/fda_inspections/ototronix-llc/ad04a5b1-28da-49c6-9ec9-80c05ac58c2c)

Company: https://www.keypedia.com/companies/ototronix-llc/4825940d-799f-43bb-acd4-21d7d4297b2d

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