FDA Inspection 837467 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3010195960

The FDA completed an inspection of Biomat USA, Inc. on June 5, 2013 in Laredo, 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
June 5, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Laredo, TX (United States)