FDA Inspection 792878 — Seraplex Inc

Seraplex Inc — FEI 1000124914

The FDA completed an inspection of Seraplex Inc on July 25, 2012 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
July 25, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pasadena, CA (United States)