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FDA Inspection 715262 — Fresenius Kabi USA LLC

Fresenius Kabi USA LLC — FEI 1450022

The FDA completed an inspection of Fresenius Kabi USA LLC on March 18, 2011 in Melrose Park, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 18, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Melrose Park, IL (United States)

Facility

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  • 1075139 (NAI Mon Dec 03 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
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