FDA Inspection 1106731 — Grifols Biomat

Grifols Biomat — FEI 3002717772

The FDA completed an inspection of Grifols Biomat on September 19, 2019 in Reading, PA. 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 19, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Reading, PA (United States)