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FDA Inspection 578325 — Biomat USA Inc

Biomat USA Inc — FEI 2376147

The FDA completed an inspection of Biomat USA Inc on April 24, 2009 in Lafayette, LA. 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
April 24, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lafayette, LA (United States)

Facility

Other inspections at this facility

  • 1201897 (VAI Tue Apr 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1009373 (NAI Fri Apr 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885925 (VAI Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 760159 (NAI Wed Dec 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources