FDA Inspection 1009636 — Biomat USA, Inc

Biomat USA, Inc — FEI 1037531

The FDA completed an inspection of Biomat USA, Inc on April 7, 2017 in Tuscaloosa, AL. 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
April 7, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tuscaloosa, AL (United States)