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

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Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on August 8, 2025, issued by the New England District Office, covering medical devices & rad health.

Company: Fresenius Kabi USA, LLC
Inspection Date: August 8, 2025
Product Type: Medical Devices & Rad Health
Office: New England District Office

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ID · 2df65180-4048-42b2-ae51-a41cd9e999c8

Violation Codes4

21 CFR 820.100(a)21 CFR 820.30(c)21 CFR 820.30(g)21 CFR 820.30(i)

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