FDA Inspection 1012286 — OneBlood, Inc.

OneBlood, Inc. — FEI 1000132464

The FDA completed an inspection of OneBlood, Inc. on February 2, 2017 in Fort Walton Beach, 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
February 2, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Walton Beach, FL (United States)