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FDA Inspection 747451 — Biomat USA, Inc

Biomat USA, Inc — FEI 3007272567

The FDA completed an inspection of Biomat USA, Inc on September 21, 2011 in Portland, OR. 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 21, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)

Facility

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FDA data resources