FDA Inspection 1051871 — OneBlood, Inc.

OneBlood, Inc. — FEI 3003991501

The FDA completed an inspection of OneBlood, Inc. on Mar 21, 2018 in Port St Lucie, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 21, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Port St Lucie, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.