# FDA Inspection 1229851 - Fresenius Kabi USA, LLC - February 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/0d2c4406-a247-4fb1-b873-9ef934f41f8c
Source feed: FDA_Inspections

> FDA Inspection 1229851 for Fresenius Kabi USA, LLC on February 08, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1229851
- Company Name: Fresenius Kabi USA, LLC
- Inspection Date: 2024-02-08
- 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.keypedia.com/companies/fresenius-kabi-usa-llc/6b662e1b-3996-48b4-a517-0d555d32a380

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