FDA Inspection 664475 — Biomat USA Inc

Biomat USA Inc — FEI 3005523333

The FDA completed an inspection of Biomat USA Inc on May 28, 2010 in Richmond, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 28, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Richmond, VA (United States)

Citations

IDCFRDescription
33321 CFR 640.64(e)Prevention of contamination
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs