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FDA Inspection 1079880 — Grifols Diagnostic Solutions, Inc.

Grifols Diagnostic Solutions, Inc. — FEI 1000124057

The FDA completed an inspection of Grifols Diagnostic Solutions, Inc. on February 15, 2019 in Emeryville, CA. 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
February 15, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Emeryville, CA (United States)

Facility

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FDA data resources