# FDA Inspection 983423 - Cordis US Corp - March 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/cordis-us-corp/e445f50f-d3ad-4ec3-86ce-821e5a9ec200
Source feed: FDA_Inspections

> FDA Inspection 983423 for Cordis US Corp on March 31, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983423
- Company Name: Cordis US Corp
- Inspection Date: 2016-03-31
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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