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FDA Inspection 699913 — Biomat USA Inc

Biomat USA Inc — FEI 2177767

The FDA completed an inspection of Biomat USA Inc on December 1, 2010 in Kenosha, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 1, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kenosha, WI (United States)

Facility

Other inspections at this facility

  • 1097910 (NAI Wed Jul 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 944941 (NAI Fri Sep 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 836330 (NAI Thu Jun 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 554283 (NAI Thu Dec 18 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources