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FDA Inspection
•Fresenius Kabi USA, LLC•February 13, 2026

Fresenius Kabi USA, LLC – FDA Inspection, Feb 13, 2026

Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on February 13, 2026, issued by the Atlanta District Office, covering human drugs.

Company
Fresenius Kabi USA, LLC
Inspection Date
February 13, 2026
Product Type
Human Drugs
Office
Atlanta District Office
People
  • Ankur C. Patel
  • Karishma G. Gopaul (FDA Associated Person)
  • Yvins Dezan
View Company Profile

ID · 886cf647-7fa8-4158-9e3f-40cf13a32dac

Inspection Facts

Inspection number
1303090
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Fresenius Kabi USA, LLC

6
DateClassificationOfficeProject area
February 8, 2024VAICenter for Devices and Radiological HealthCompliance: Devices
June 13, 2023OAICenter for Drug Evaluation and ResearchGeneric Drug Evaluation
February 5, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 18, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
June 24, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Fresenius Kabi USA, LLC
  • FDA Inspection 1229851 - 2024-02-08
  • FDA Inspection 1208507 - 2023-06-13
  • FDA Inspection 1079248 - 2019-02-05
  • FDA Inspection 1026620 - 2017-08-18
  • FDA Inspection 988705 - 2016-06-24

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