FDA Inspection 1105254 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3003733819

The FDA completed an inspection of Biomat USA, Inc. on August 30, 2019 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) (NAI)
End Date
August 30, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Indianapolis, IN (United States)