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FDA Inspection 646575 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1044773

The FDA completed an inspection of Biomat USA, Inc. on February 8, 2010 in Clarksville, TN. 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
February 8, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Clarksville, TN (United States)

Facility

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FDA data resources