FDA Inspection 945820 — OneBlood, Inc.

OneBlood, Inc. — FEI 3004027599

The FDA completed an inspection of OneBlood, Inc. on October 20, 2015 in Venice, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 20, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Venice, FL (United States)

Citations

IDCFRDescription
5721 CFR 606.60(a)Maintain and clean equipment
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs