FDA Inspection 1067687 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006213838

The FDA completed an inspection of Biomat USA, Inc. on Sep 20, 2018 in Indianapolis, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 20, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Indianapolis, IN (United States)