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FDA Inspection
•Fresenius Kabi USA, LLC•August 18, 2017

Fresenius Kabi USA, LLC – FDA Inspection, Aug 18, 2017

Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on August 18, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Fresenius Kabi USA, LLC
Inspection Date
August 18, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Samuel L. Murray (Company Rep)
View Company Profile

ID · c0154c8a-66e0-490c-b1d5-2d7fd7926336

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1026620
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Fresenius Kabi USA, LLC

6
DateClassificationOfficeProject area
February 13, 2026Not classifiedAtlanta District Office
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
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 1303090 - 2026-02-13
  • FDA Inspection 1229851 - 2024-02-08
  • FDA Inspection 1208507 - 2023-06-13
  • FDA Inspection 1079248 - 2019-02-05
  • FDA Inspection 988705 - 2016-06-24

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