# Fresenius Kabi USA, LLC – FDA Inspection, Feb 8, 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 of Fresenius Kabi USA, LLC, February 08, 2024. Classification: Voluntary Action Indicated (VAI). 6 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 988705 - 2016-06-24](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/e7df94d1-c707-4569-b8db-0bd30fcf97bf)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/inga-m-warr/f27805b8-c2ba-4af5-bf5e-ff2e2f511ec1)

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