FDA Inspection 971958 — OneBlood, Inc.

OneBlood, Inc. — FEI 3003991501

The FDA completed an inspection of OneBlood, Inc. on May 5, 2016 in Port St Lucie, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 5, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Port St Lucie, FL (United States)