# FDA Inspection 1206544 - Fresenius U.S.A. Manufacturing - May 08, 2023

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing/9eefc72b-bfbf-4ead-a043-1938d2da3599
Source feed: FDA_Inspections

> FDA Inspection 1206544 for Fresenius U.S.A. Manufacturing on May 08, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1206544
- Company Name: Fresenius U.S.A. Manufacturing
- Inspection Date: 2023-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/fresenius-usa-manufacturing/d7fc621f-9400-4de0-bc05-4542deabe147

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