FDA Inspection 1028285 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 1626579

The FDA completed an inspection of Biomat USA, Inc. on September 14, 2017 in El Paso, 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
September 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
El Paso, TX (United States)