# FDA Inspection 587334 - Cordis Neurovascular, Inc. - May 08, 2009

Source: https://www.keypedia.com/records/fda_inspections/cordis-neurovascular-inc/8aa78740-db97-4da2-9c15-3ebddd3642fc
Source feed: FDA_Inspections

> FDA Inspection 587334 for Cordis Neurovascular, Inc. on May 08, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 587334
- Company Name: Cordis Neurovascular, Inc.
- Inspection Date: 2009-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 587334 - 2009-05-08](https://www.keypedia.com/records/fda_inspections/cordis-neurovascular-inc/2229f683-ffdb-46a5-94e4-1a8fa8c17a26)
- [FDA Inspection 587334 - 2009-05-08](https://www.keypedia.com/records/fda_inspections/cordis-neurovascular-inc/81a780b5-0d3e-41f7-b6db-1a6ffd9a6278)

Company: https://www.keypedia.com/companies/cordis-neurovascular-inc/e00001f2-6937-424a-a7af-64a609da0cab

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