FDA Inspection 809389 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005865223

The FDA completed an inspection of Biomat USA, Inc. on Nov 30, 2012 in Eagle Pass, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 30, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Eagle Pass, TX (United States)