FDA Inspection 1232805 — Seraplex Inc

Seraplex Inc — FEI 1000124914

The FDA completed an inspection of Seraplex Inc on March 8, 2024 in Pasadena, CA. 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
March 8, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pasadena, CA (United States)