# FDA Inspection 640523 - Fresenius Kabi USA, LLC - January 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/fresenius-kabi-usa-llc/d5e3d4e7-ffcf-4998-8061-9a56dc8540d8
Source feed: FDA_Inspections

> FDA Inspection 640523 for Fresenius Kabi USA, LLC on January 21, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 640523
- Company Name: Fresenius Kabi USA, LLC
- Inspection Date: 2010-01-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/fresenius-kabi-usa-llc/b7c42c60-8a6f-4ccf-8db1-03c0263b3887

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