FDA Inspection 755174 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1629787

The FDA completed an inspection of Biomat USA, Inc. on December 1, 2011 in El Paso, TX. 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
December 1, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
El Paso, TX (United States)

Citations

IDCFRDescription
325821 CFR 640.63(d)Unreliable answers