FDA Inspection 753878 — Biomat USA Inc

Biomat USA Inc — FEI 3005601885

The FDA completed an inspection of Biomat USA Inc on Nov 18, 2011 in Des Moines, IA. 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
Nov 18, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Des Moines, IA (United States)

Citations

IDCFRDescription
4121 CFR 606.40(a)(1)Provide space for examination