FDA Inspection 905531 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3005622193

The FDA completed an inspection of Biomat USA, Inc. on November 20, 2014 in San Antonio, 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
November 20, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Antonio, TX (United States)