FDA Inspection 707745 — Biomat USA Inc.

Biomat USA Inc. — FEI 3006192337

The FDA completed an inspection of Biomat USA Inc. on January 28, 2011 in Sioux Falls, SD. 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
January 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Sioux Falls, SD (United States)