FDA Inspection 930547 — Grifols Biomat

Grifols Biomat — FEI 3002717772

The FDA completed an inspection of Grifols Biomat on June 11, 2015 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
June 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Reading, PA (United States)