FDA Inspection 1303090 — Fresenius Kabi USA, LLC

Fresenius Kabi USA, LLC — FEI 3008887707

The FDA completed an inspection of Fresenius Kabi USA, LLC on February 13, 2026 in Wilson, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wilson, NC (United States)