FDA Inspection 1109813 — AGC Biologics, Inc.

AGC Biologics, Inc. — FEI 3000209996

The FDA completed an inspection of AGC Biologics, Inc. on October 15, 2018 in Bothell, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 15, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bothell, WA (United States)