# FDA Inspection 1019824 - Fresenius Kabi USA LLC - July 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/d2c8fc67-5e12-4f94-80ad-de6d402f6ac3
Source feed: FDA_Inspections

> FDA Inspection 1019824 for Fresenius Kabi USA LLC on July 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019824
- Company Name: Fresenius Kabi USA LLC
- Inspection Date: 2017-07-20
- 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/fresenius-kabi-usa-llc/27355905-dcff-4134-8adc-7a3e64247361

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