# FDA Inspection 1173562 - Cordis US Corp - June 29, 2022

Source: https://www.keypedia.com/records/fda_inspections/cordis-us-corp/0aef5089-7e44-4783-b26e-9c741c09f6ff
Source feed: FDA_Inspections

> FDA Inspection 1173562 for Cordis US Corp on June 29, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1173562
- Company Name: Cordis US Corp
- Inspection Date: 2022-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1173562 - 2022-06-29](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/8cb7bcb6-7002-4e73-bfd0-7c26b57a473a)
- [FDA Inspection 1037525 - 2018-01-12](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/e3668211-3e8e-4199-8605-7294d6c42abf)
- [FDA Inspection 979906 - 2016-07-06](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/42bfbf41-32d9-4c67-bbf8-7a7988b6b744)
- [FDA Inspection 979906 - 2016-07-06](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/6287234f-7bab-4f6d-8afb-abb464f35bc6)
- [FDA Inspection 983423 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/cordis-us-corp/2979687c-b443-4f40-b7aa-99a5bab26e73)

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

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