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FDA Inspection 849552 — Biomat USA Inc

Biomat USA Inc — FEI 3023457

The FDA completed an inspection of Biomat USA Inc on September 19, 2013 in Salem, OR. 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
September 19, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salem, OR (United States)

Facility

Other inspections at this facility

  • 1118882 (NAI Thu Jan 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1027767 (VAI Thu Oct 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 930472 (NAI Wed Jun 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 794880 (VAI Thu Aug 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 655320 (NAI Thu Feb 11 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources