FDA Inspection 1101884 — Biomat USA, Inc

Biomat USA, Inc — FEI 1038382

The FDA completed an inspection of Biomat USA, Inc on July 11, 2019 in Asheville, 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 11, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Asheville, NC (United States)