FDA Inspection 1316578 — Grifols Biomat, INC

Grifols Biomat, INC — FEI 3022888428

The FDA completed an inspection of Grifols Biomat, INC on May 11, 2026 in Saint Petersburg, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 11, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Petersburg, FL (United States)

Citations

IDCFRDescription
15521 CFR 606.160(b)Required records