# Cordis US Corp - Inspection Records

Source: https://www.keypedia.com/companies/cordis-us-corp/0356db58-939c-4049-b5a9-010a14550d56

> Inspection records and compliance data for Cordis US Corp in Miami Lakes, Florida. Access full analysis and detailed observations.

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## Details

- Name: Cordis US Corp
- FEI Number: 1016427
- City: Miami Lakes
- State: Florida
- Country Name: United States
- Address Line 1: 14201 Nw 60th Ave
- Zip Code: 33014

## Related Documents

- [483 - Cordis US Corp - 2022-06-29](https://www.keypedia.com/records/483/cordis-us-corp/2f618886-300c-4bdb-9435-92f09ba6a965) — source: FDA, date: June 29, 2022
- [FDA Inspection 1173562 - Cordis US Corp - 2022-06-29](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/0aef5089-7e44-4783-b26e-9c741c09f6ff) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2022
- [FDA Inspection 1173562 - Cordis US Corp - 2022-06-29](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/8cb7bcb6-7002-4e73-bfd0-7c26b57a473a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2022
- [FDA Inspection 1037525 - Cordis US Corp - 2018-01-12](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/e3668211-3e8e-4199-8605-7294d6c42abf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 12, 2018
- [FDA Inspection 979906 - Cordis US Corp - 2016-07-06](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/42bfbf41-32d9-4c67-bbf8-7a7988b6b744) — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2016
- [FDA Inspection 979906 - Cordis US Corp - 2016-07-06](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/6287234f-7bab-4f6d-8afb-abb464f35bc6) — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2016
- [EIR - Cordis US Corp - 2016-03-31](https://www.keypedia.com/records/eir/cordis-us-corp/72f88d8c-dcc3-4138-95f2-64b9fb275f5f) — source: FDA, date: March 31, 2016
- [FDA Inspection 983423 - Cordis US Corp - 2016-03-31](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/e445f50f-d3ad-4ec3-86ce-821e5a9ec200) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2016
- [FDA Inspection 983423 - Cordis US Corp - 2016-03-31](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/2979687c-b443-4f40-b7aa-99a5bab26e73) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2016
- [FDA Inspection 923766 - Cordis US Corp - 2015-05-08](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/88b36740-b489-446e-bcb9-4c2f437e3580) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2015
- [EIR - Cordis US Corp - 2014-01-30](https://www.keypedia.com/records/eir/cordis-us-corp/82b14bc7-41fc-469f-836f-f742b8137f8f) — source: FDA, date: January 30, 2014
- [FDA Inspection 867722 - Cordis US Corp - 2014-01-30](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/45822fee-abf7-4fc2-8a02-67415f28864a) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2014
- [FDA Inspection 859408 - Cordis US Corp - 2013-12-18](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/bb602238-dac3-49c6-af40-584c7848e400) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2013

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