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FDA Inspection 567141 — Biomat USA, Inc

Biomat USA, Inc — FEI 2072896

The FDA completed an inspection of Biomat USA, Inc on March 5, 2009 in Laredo, TX. 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
March 5, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Laredo, TX (United States)

Facility

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