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FDA Inspection 801013 — Kedrion Biopharma Inc.

Kedrion Biopharma Inc. — FEI 3003683714

The FDA completed an inspection of Kedrion Biopharma Inc. on August 2, 2012 in Melville, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 2, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Melville, NY (United States)

Facility

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FDA data resources