# Otodynamics Limited – FDA Inspection, Feb 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/otodynamics-limited/e164e708-c8fe-4c0e-bd62-4491418b1276
Source feed: FDA_Inspections

> FDA inspection 1003852 of Otodynamics Limited, February 03, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003852
- Company Name: Otodynamics Limited
- Inspection Date: 2017-02-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- FDA Inspection 1261981 - 2025-01-09
- [FDA Inspection 1065829 - 2018-09-13](https://www.keypedia.com/records/fda_inspections/otodynamics-limited/5b19f0ec-9852-4d64-9748-5a3255ec7f2c)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/otodynamics-limited/7928e076-b9e2-4069-be0e-b127e9aa7dd5

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