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FDA Inspection
•Fresenius Kabi USA, LLC•March 18, 2022

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

Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on March 18, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company
Fresenius Kabi USA, LLC
Inspection Date
March 18, 2022
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · d2b4d46e-9328-4d99-a1eb-02ce8813fb69

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1164862
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Fresenius Kabi USA, LLC

2
DateClassificationOfficeProject area
August 8, 2025OAICompliance: Devices
September 7, 2023OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Fresenius Kabi USA, LLC
  • FDA Inspection 1278050 - 2025-08-08
  • FDA Inspection 1217750 - 2023-09-07

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