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FDA Inspection 640925 — Biomat USA, Inc

Biomat USA, Inc — FEI 1038382

The FDA completed an inspection of Biomat USA, Inc on December 11, 2009 in Asheville, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Asheville, NC (United States)

Facility

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FDA data resources