# Fresenius U.S.A. Manufacturing – FDA Inspection, May 8, 2023

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing/d76d9ac0-8aa1-4b15-bbc5-0fc591907b95
Source feed: FDA_Inspections

> FDA inspection 1206544 of Fresenius U.S.A. Manufacturing, May 08, 2023. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## 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)
- 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 1016670 - 2017-06-30](https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing/d641c6c1-3e08-4451-a67c-5668a9114667)
- FDA Inspection 809863 - 2012-12-27
- FDA Inspection 667215 - 2010-06-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-j-gasparovich/478888db-d4b3-481a-89f5-ee234a160f07)

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