# FDA Inspection 812020 - CareFusion 303, Inc. - December 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/49b88cc2-2c1c-4245-86a2-42935cc5c2be
Source feed: FDA_Inspections

> FDA Inspection 812020 for CareFusion 303, Inc. on December 18, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 812020
- Company Name: CareFusion 303, Inc.
- Inspection Date: 2012-12-18
- 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/carefusion-303-inc/e44e5a89-d532-4564-ac5f-1aff2b7d8974

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