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FDA Inspection
•Fresenius USA Manufacturing, Inc•October 18, 2024

Fresenius USA Manufacturing, Inc – FDA Inspection, Oct 18, 2024

Record Details

This FDA Inspection record concerns Fresenius USA Manufacturing, Inc, with an inspection on October 18, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Fresenius USA Manufacturing, Inc
Inspection Date
October 18, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Benjamin E. Bowen (Investigator)
View Company Profile

ID · d49f004f-328e-43b9-ac7b-3fed9a7a764a

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1251719
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Fresenius USA Manufacturing, Inc

5
DateClassificationOfficeProject area
September 19, 2025Not classifiedNew Orleans District Office
December 7, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
June 26, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 12, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 6, 2017VAINew Orleans District OfficeNew Drug Evaluation
Other documents for Fresenius USA Manufacturing, Inc
  • FDA Inspection 1284734 - 2025-09-19
  • FDA Inspection 1195086 - 2022-12-07
  • FDA Inspection 1124187 - 2020-06-26
  • FDA Inspection 1110322 - 2019-09-12
  • FDA Inspection 1028853 - 2017-10-06

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