# FDA Inspection 542247 - CareFusion DR 203 LTD - October 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/carefusion-dr-203-ltd/5a7ea0bf-8f8d-4c32-b0a0-3c19e2413d3f
Source feed: FDA_Inspections

> FDA Inspection 542247 for CareFusion DR 203 LTD on October 30, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 542247
- Company Name: CareFusion DR 203 LTD
- Inspection Date: 2014-10-30
- Classification: No Action Indicated (NAI)
- 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-dr-203-ltd/e36e3765-fd82-4a83-adfb-addff0f9543d

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