FDA Inspection 809386 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1626798

The FDA completed an inspection of Biomat USA, Inc. on Nov 28, 2012 in Del Rio, 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 28, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Del Rio, TX (United States)