# FDA Inspection 1278050 - Fresenius Kabi USA, LLC - August 08, 2025

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/2df65180-4048-42b2-ae51-a41cd9e999c8
Source feed: FDA_Inspections

> FDA Inspection 1278050 for Fresenius Kabi USA, LLC on August 08, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1278050
- Company Name: Fresenius Kabi USA, LLC
- Inspection Date: 2025-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

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

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144