# Fresenius USA, Inc. – FDA Inspection, Nov 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-inc/02ad0e64-41a3-4c0e-8899-9ae97a7bad6d
Source feed: FDA_Inspections

> FDA inspection 697563 of Fresenius USA, Inc., November 16, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 697563
- Company Name: Fresenius USA, Inc.
- Inspection Date: 2010-11-16
- 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

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- [FDA Inspection 822364 - 2013-02-22](https://www.keypedia.com/records/fda_inspections/fresenius-usa-inc/fc5dcf43-7d33-4536-b14d-94fc71aa2ce4)
- [FDA Inspection 755564 - 2011-12-07](https://www.keypedia.com/records/fda_inspections/fresenius-usa-inc/dc15f84f-0bea-4517-828f-21ce8400969e)

Company: https://www.keypedia.com/companies/fresenius-usa-inc/3cc6adda-f320-4810-b4a0-0cf6c6321f86

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