# Fresenius U.S.A. Manufacturing – FDA Inspection, Jun 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing/d641c6c1-3e08-4451-a67c-5668a9114667
Source feed: FDA_Inspections

> FDA inspection 1016670 of Fresenius U.S.A. Manufacturing, June 30, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016670
- Company Name: Fresenius U.S.A. Manufacturing
- Inspection Date: 2017-06-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1206544 - 2023-05-08](https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing/d76d9ac0-8aa1-4b15-bbc5-0fc591907b95)
- FDA Inspection 809863 - 2012-12-27
- FDA Inspection 667215 - 2010-06-15

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

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