# Fresenius USA, Inc. – FDA Inspection, Dec 7, 2011

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-inc/dc15f84f-0bea-4517-828f-21ce8400969e
Source feed: FDA_Inspections

> FDA inspection 755564 of Fresenius USA, Inc., December 07, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 806 and 820. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 755564
- Company Name: Fresenius USA, Inc.
- Inspection Date: 2011-12-07
- 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: 2

## Related Documents

- FDA Inspection 940274 - 2015-08-27
- FDA Inspection 864135 - 2014-01-30
- FDA Inspection 822918 - 2013-03-14
- [FDA Inspection 822364 - 2013-02-22](https://www.keypedia.com/records/fda_inspections/fresenius-usa-inc/fc5dcf43-7d33-4536-b14d-94fc71aa2ce4)
- FDA Inspection 748172 - 2011-10-24

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