# FDA Inspection 739660 - Cordis LLC - August 16, 2011

Source: https://www.keypedia.com/records/fda_inspections/cordis-llc/9044ea6d-245f-421f-ab45-1f4ca60e6be2
Source feed: FDA_Inspections

> FDA Inspection 739660 for Cordis LLC on August 16, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 739660
- Company Name: Cordis LLC
- Inspection Date: 2011-08-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 685359 - 2010-10-13](https://www.keypedia.com/records/fda_inspections/cordis-llc/e8d3bb0f-ee80-4a8e-9a17-9f0c0d6a414a)
- [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