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FDA Inspection 935336 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005600120

The FDA completed an inspection of Biomat USA, Inc. on July 17, 2015 in Portland, 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
July 17, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)

Facility

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  • 989350 (NAI Mon Oct 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847837 (NAI Wed Sep 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 681879 (NAI Tue Sep 21 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources