# Cochlear Americas Inc. - Inspection Records

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

> Inspection records and compliance data for Cochlear Americas Inc. in Lone Tree, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Cochlear Americas Inc.
- FEI Number: 3005900820
- City: Lone Tree
- State: Colorado
- Country Name: United States
- Address Line 1: 10350 Park Meadows Dr
- Zip Code: 80124

## Related Documents

- [483 - Cochlear Americas Inc. - 2021-10-21](https://www.keypedia.com/records/483/cochlear-americas-inc/097e786d-e3b6-40a3-b4ff-93e96aba01a8) — source: FDA, date: October 21, 2021
- [FDA Inspection 1155204 - Cochlear Americas Inc. - 2021-10-21](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/9db55583-bf90-4f15-ae7b-f18a8d612bd9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 21, 2021
- [FDA Inspection 1078710 - Cochlear Americas Inc. - 2018-11-28](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/59a1fe7f-a98b-49c6-980a-4980322a7742) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2018
- [FDA Inspection 1078710 - Cochlear Americas Inc. - 2018-11-28](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/dd5ed257-3ed1-492c-a52d-ae6140dfc901) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2018
- [EIR - Cochlear Americas Inc. - 2018-02-22](https://www.keypedia.com/records/eir/cochlear-americas-inc/513d3fd5-762c-4ed8-9f96-cdc020214105) — source: FDA, date: February 22, 2018
- [483 - Cochlear Americas Inc. - 2018-02-22](https://www.keypedia.com/records/483/cochlear-americas-inc/e1d96993-d0f1-4a88-8746-4266a4878897) — source: FDA, date: February 22, 2018
- [FDA Inspection 1042149 - Cochlear Americas Inc. - 2018-02-22](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/a702e54f-4b20-49de-8880-322882ddc910) — classification: Official Action Indicated (OAI), source: FDA, date: February 22, 2018
- [FDA Inspection 855809 - Cochlear Americas Inc. - 2013-10-22](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/b720ea3b-b626-4117-9db2-c9a76662913e) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2013
- [FDA Inspection 855809 - Cochlear Americas Inc. - 2013-10-22](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/ed04fef5-71f7-49a6-a74e-e84a68bf3400) — classification: No Action Indicated (NAI), source: FDA, date: October 22, 2013
- [FDA Inspection 849948 - Cochlear Americas Inc. - 2013-09-18](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/2e41bc27-5777-43bc-b0a5-d7fbd294305d) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2013
- [FDA Inspection 582805 - Cochlear Americas Inc. - 2009-05-12](https://www.keypedia.com/records/fda_inspections/cochlear-americas-inc/ebef671e-d31d-4c6c-aec0-45f6572994b0) — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2009

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