# FDA Inspection 809863 - Fresenius U.S.A. Manufacturing - December 27, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/fresenius-usa-manufacturing/f7fdd9f5-68c8-4d97-9aa5-65638e62f242/
Source feed: FDA_Inspections

> FDA Inspection 809863 for Fresenius U.S.A. Manufacturing on December 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809863
- Company Name: Fresenius U.S.A. Manufacturing
- Inspection Date: 2012-12-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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