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FDA Inspection 829212 — Biomat USA Inc

Biomat USA Inc — FEI 3003853409

The FDA completed an inspection of Biomat USA Inc on April 26, 2013 in Portsmouth, VA. 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
April 26, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portsmouth, VA (United States)

Facility

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FDA data resources