FDA Inspection 615024 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006687044

The FDA completed an inspection of Biomat USA, Inc. on September 30, 2009 in Jacksonville, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 30, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
9821 CFR 606.100(c)Thorough investigations