FDA Inspection 1099570 — Biomat USA, Inc

Biomat USA, Inc — FEI 3006784517

The FDA completed an inspection of Biomat USA, Inc on July 18, 2019 in Raleigh, NC. 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
July 18, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Raleigh, NC (United States)