FDA Inspection 1102088 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005600120

The FDA completed an inspection of Biomat USA, Inc. on September 11, 2019 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
September 11, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Portland, OR (United States)