# FDA Inspection 793900 - Cordis US Corp - July 03, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/cordis-us-corp/da539412-7582-429f-9d37-d7406ff3b608
Source feed: FDA_Inspections

> FDA Inspection 793900 for Cordis US Corp on July 03, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 793900
- Company Name: Cordis US Corp
- Inspection Date: 2012-07-03
- 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.globalkeysolutions.net/companies/cordis-us-corp/0356db58-939c-4049-b5a9-010a14550d56

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