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

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing-inc/d49f004f-328e-43b9-ac7b-3fed9a7a764a
Source feed: FDA_Inspections

> FDA inspection 1251719 of Fresenius USA Manufacturing, Inc, October 18, 2024. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1251719
- Company Name: Fresenius USA Manufacturing, Inc
- Inspection Date: 2024-10-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- 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](https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing-inc/56e86173-71a4-416b-83ec-6bc5c4e27b4e)

## Related Officers

- [Investigator](https://www.keypedia.com/people/benjamin-e-bowen/7fdc5755-0d5d-45c9-93a0-3cb928156c1d)

Company: https://www.keypedia.com/companies/fresenius-usa-manufacturing-inc/6a1a5f30-4674-4964-a33e-c6401405fba9

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7