FDA Inspection 1057030 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3002672568

The FDA completed an inspection of Biomat USA, Inc. on May 30, 2018 in Everett, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 30, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Everett, WA (United States)