FDA Inspection 680996 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006576463

The FDA completed an inspection of Biomat USA, Inc. on September 10, 2010 in Little Rock, AR. 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 10, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Little Rock, AR (United States)