FDA Inspection 756113 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003908050

The FDA completed an inspection of Biomat USA, Inc on December 12, 2011 in Houston, TX. 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
December 12, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Houston, TX (United States)