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FDA Inspection 885925 — Biomat USA Inc

Biomat USA Inc — FEI 2376147

The FDA completed an inspection of Biomat USA Inc on July 1, 2014 in Lafayette, LA. 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
July 1, 2014
Fiscal Year
2014
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))
  • 760159 (NAI Wed Dec 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 578325 (NAI Fri Apr 24 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources