# FDA Inspection 1078710 - Cochlear Americas Inc. - November 28, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/cochlear-americas-inc/dd5ed257-3ed1-492c-a52d-ae6140dfc901
Source feed: FDA_Inspections

> FDA Inspection 1078710 for Cochlear Americas Inc. on November 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078710
- Company Name: Cochlear Americas Inc.
- Inspection Date: 2018-11-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1078710 - 2018-11-28](https://www.globalkeysolutions.net/records/fda_inspections/cochlear-americas-inc/59a1fe7f-a98b-49c6-980a-4980322a7742)
- [FDA Inspection 1042149 - 2018-02-22](https://www.globalkeysolutions.net/records/fda_inspections/cochlear-americas-inc/a702e54f-4b20-49de-8880-322882ddc910)
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- [FDA Inspection 855809 - 2013-10-22](https://www.globalkeysolutions.net/records/fda_inspections/cochlear-americas-inc/ed04fef5-71f7-49a6-a74e-e84a68bf3400)

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

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