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FDA Inspection 817237 — OneBlood, Inc.

OneBlood, Inc. — FEI 1070206

The FDA completed an inspection of OneBlood, Inc. on January 30, 2013 in Ocala, FL. 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
January 30, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ocala, FL (United States)

Facility

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FDA data resources