FDA Inspection 943172 — Biomat USA Inc

Biomat USA Inc — FEI 3001451631

The FDA completed an inspection of Biomat USA Inc on September 4, 2015 in Carbondale, IL. 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
September 4, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carbondale, IL (United States)