# FDA Inspection 753121 - Ototronix, LLC - November 10, 2011

Source: https://www.keypedia.com/records/fda_inspections/ototronix-llc/3fece1e1-0da0-4251-ab53-c9d1efd6776e
Source feed: FDA_Inspections

> FDA Inspection 753121 for Ototronix, LLC on November 10, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 753121
- Company Name: Ototronix, LLC
- Inspection Date: 2011-11-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 842199 - 2013-08-16](https://www.keypedia.com/records/fda_inspections/ototronix-llc/3e032e2b-08aa-47ea-887e-75173a67383c)
- [FDA Inspection 842199 - 2013-08-16](https://www.keypedia.com/records/fda_inspections/ototronix-llc/3256321f-d2d9-4621-9d92-ed3a8be78ab9)
- [FDA Inspection 753121 - 2011-11-10](https://www.keypedia.com/records/fda_inspections/ototronix-llc/e51be644-9614-4d60-9849-d2a8a1090370)

Company: https://www.keypedia.com/companies/ototronix-llc/496d228b-b4f3-4f30-9696-6d19d3d19ca1

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