FDA Inspection 774405 — Biomat USA, Inc

Biomat USA, Inc — FEI 1876548

The FDA completed an inspection of Biomat USA, Inc on Mar 16, 2012 in Colorado Springs, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 16, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Colorado Springs, CO (United States)

Citations

IDCFRDescription
9821 CFR 606.100(c)Thorough investigations