FDA Inspection 863406 — Biomat USA Inc

Biomat USA Inc — FEI 2077733

The FDA completed an inspection of Biomat USA Inc on Jan 28, 2014 in Reseda, CA. 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
Jan 28, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Reseda, CA (United States)