FDA Inspection 747161 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3000718117

The FDA completed an inspection of Biomat USA, Inc. on September 28, 2011 in Anderson, IN. 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 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Anderson, IN (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report