# FDA Inspection 1064813 - CareFusion 303, Inc. - September 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/21cd551f-a6f2-4cc8-8e02-e7aa779bcb8e
Source feed: FDA_Inspections

> FDA Inspection 1064813 for CareFusion 303, Inc. on September 06, 2018. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064813
- Company Name: CareFusion 303, Inc.
- Inspection Date: 2018-09-06
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: 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