# Cochlear Americas Inc. – FDA Inspection, Oct 21, 2021

Source: https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/9db55583-bf90-4f15-ae7b-f18a8d612bd9
Source feed: FDA_Inspections

> FDA inspection 1155204 of Cochlear Americas Inc., October 21, 2021. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1155204
- Company Name: Cochlear Americas Inc.
- Inspection Date: 2021-10-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1078710 - 2018-11-28](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/dd5ed257-3ed1-492c-a52d-ae6140dfc901)
- [FDA Inspection 1042149 - 2018-02-22](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/f52c5908-6cf3-472f-b7bb-98803aa99204)
- FDA Inspection 855809 - 2013-10-22
- FDA Inspection 849948 - 2013-09-18
- FDA Inspection 582805 - 2009-05-12

Company: https://www.keypedia.com/companies/cochlear-americas-inc/87342f6e-3f58-4bea-b41f-0ab2088226df

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