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FDA Inspection 761209 — Biomat USA, Inc

Biomat USA, Inc — FEI 1643256

The FDA completed an inspection of Biomat USA, Inc on October 26, 2011 in McAllen, TX. 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
October 26, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
McAllen, TX (United States)

Facility

Other inspections at this facility

  • 1098274 (NAI Fri Jun 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 960815 (NAI Wed Jan 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867833 (NAI Thu Feb 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 626356 (VAI Thu Oct 22 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources