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FDA Inspection 679477 — Biomat USA, Inc

Biomat USA, Inc — FEI 3007198312

The FDA completed an inspection of Biomat USA, Inc on September 8, 2010 in Cincinnati, OH. 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
September 8, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cincinnati, OH (United States)

Facility

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FDA data resources