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FDA Inspection 988679 — Biomat USA Inc

Biomat USA Inc — FEI 3000210606

The FDA completed an inspection of Biomat USA Inc on October 10, 2016 in Rexburg, ID. 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
October 10, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rexburg, ID (United States)

Facility

Other inspections at this facility

  • 1105865 (NAI Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934720 (NAI Wed Jul 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 843415 (NAI Wed Aug 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 707994 (NAI Thu Jan 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 601977 (NAI Thu Jun 18 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources