FDA Inspection 1109813 — AGC Biologics, Inc.

AGC Biologics, Inc. — FEI 3000209996

The FDA completed an inspection of AGC Biologics, Inc. on Oct 15, 2018 in Bothell, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

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

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