# FDA Inspection 685359 - Cordis LLC - October 13, 2010

Source: https://www.keypedia.com/records/fda_inspections/cordis-llc/e8d3bb0f-ee80-4a8e-9a17-9f0c0d6a414a
Source feed: FDA_Inspections

> FDA Inspection 685359 for Cordis LLC on October 13, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 685359
- Company Name: Cordis LLC
- Inspection Date: 2010-10-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 739660 - 2011-08-16](https://www.keypedia.com/records/fda_inspections/cordis-llc/9044ea6d-245f-421f-ab45-1f4ca60e6be2)
- [FDA Inspection 685359 - 2010-10-13](https://www.keypedia.com/records/fda_inspections/cordis-llc/d78cc85f-2cde-426a-a3a1-9e533b1446c9)

Company: https://www.keypedia.com/companies/cordis-llc/b9ad8ec3-1697-4393-8d2a-a16e19a36447

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