FDA Inspection 1118233 — Biomat USA, Inc

Biomat USA, Inc — FEI 3007272567

The FDA completed an inspection of Biomat USA, Inc on January 24, 2020 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
January 24, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)