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FDA Inspection 655320 — Biomat USA Inc

Biomat USA Inc — FEI 3023457

The FDA completed an inspection of Biomat USA Inc on February 11, 2010 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
February 11, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Salem, OR (United States)

Facility

Other inspections at this facility

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  • 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))
  • 849552 (NAI Thu Sep 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 794880 (VAI Thu Aug 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources