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FDA Inspection 816888 — Biomat USA Inc

Biomat USA Inc — FEI 1718620

The FDA completed an inspection of Biomat USA Inc on February 4, 2013 in Aurora, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 4, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aurora, CO (United States)

Facility

Other inspections at this facility

  • 1112924 (NAI Thu Nov 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1029273 (NAI Wed Sep 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 869722 (NAI Tue Mar 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 708048 (NAI Fri Jan 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources