FDA Inspection 950823 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3011535765

The FDA completed an inspection of Biomat USA, Inc. on October 23, 2015 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
October 23, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Raleigh, NC (United States)