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FDA Inspection 595771 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005600120

The FDA completed an inspection of Biomat USA, Inc. on July 9, 2009 in Portland, OR. 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
July 9, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)

Facility

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FDA data resources