FDA Inspection 915125 — Biomat USA Inc

Biomat USA Inc — FEI 3006692070

The FDA completed an inspection of Biomat USA Inc on February 5, 2015 in Moorhead, MN. 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
February 5, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Moorhead, MN (United States)