# FDA Inspection 1216357 - Fresenius Kabi USA, LLC - August 30, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/fresenius-kabi-usa-llc/6b172d0c-ba88-4cda-9500-e353ae9c96c7/
Source feed: FDA_Inspections

> FDA Inspection 1216357 for Fresenius Kabi USA, LLC on August 30, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216357
- Company Name: Fresenius Kabi USA, LLC
- Inspection Date: 2023-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/fresenius-kabi-usa-llc/f0c47fa1-3b76-4e6c-82dd-d703086bdfdc

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