FDA Inspection 703057 — OneBlood, Inc.

OneBlood, Inc. — FEI 1000143757

The FDA completed an inspection of OneBlood, Inc. on December 23, 2010 in Melbourne, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 23, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Melbourne, FL (United States)

Citations

IDCFRDescription
3121 CFR 606.20(b)Qualifications of responsible personnel
5721 CFR 606.60(a)Maintain and clean equipment
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs