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FDA Inspection
•Fresenius Kabi USA, LLC•June 29, 2018

Fresenius Kabi USA, LLC – FDA Inspection, Jun 29, 2018

Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on June 29, 2018, issued by the New York District Office, covering human drugs.

Company
Fresenius Kabi USA, LLC
Inspection Date
June 29, 2018
Product Type
Human Drugs
Office
New York District Office
People
  • Sony Mathews (FDA Associated Person)
  • William J. Leonard (Issuing Officer)
View Company Profile

ID · 4d4a8d6e-45c7-4d98-ba25-b17a681a9bc4

Inspection Facts

Inspection number
1059868
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Fresenius Kabi USA, LLC

15
DateClassificationOfficeProject area
May 14, 2026Not classifiedNew York District OfficeDrug Quality Assurance
October 13, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 30, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 12, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 30, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 15 other inspections on the company page
Other documents for Fresenius Kabi USA, LLC
  • FDA Inspection 1317954 - 2026-05-14
  • FDA Inspection 1220482 - 2023-10-13
  • FDA Inspection 1216357 - 2023-08-30
  • FDA Inspection 1099323 - 2019-08-12
  • FDA Inspection 1014707 - 2017-03-30

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