# Fresenius Kabi USA, LLC – FDA Inspection, Mar 18, 2022

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/d2b4d46e-9328-4d99-a1eb-02ce8813fb69
Source feed: FDA_Inspections

> FDA inspection 1164862 of Fresenius Kabi USA, LLC, March 18, 2022. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1164862
- Company Name: Fresenius Kabi USA, LLC
- Inspection Date: 2022-03-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1278050 - 2025-08-08](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/e6910233-1465-45b7-bb8f-21b3c1123db8)
- [FDA Inspection 1217750 - 2023-09-07](https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/d1d35133-ab0a-4318-8ebc-ce736b2a6f9d)

Company: https://www.keypedia.com/companies/fresenius-kabi-usa-llc/f0976e16-40e3-475b-8dc0-c9e721658b4a

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