FDA Inspection 1317004 — Grifols Biomat USA

Grifols Biomat USA — FEI 3021124237

The FDA completed an inspection of Grifols Biomat USA on April 23, 2026 in Worcester, MA. 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
April 23, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Worcester, MA (United States)