FDA Inspection 684478 — Biomat USA Inc

Biomat USA Inc — FEI 3006692070

The FDA completed an inspection of Biomat USA Inc on October 1, 2010 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
October 1, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Moorhead, MN (United States)