FDA Inspection 838378 — OneBlood, Inc.

OneBlood, Inc. — FEI 3003290774

The FDA completed an inspection of OneBlood, Inc. on Jun 28, 2013 in Ormond Beach, 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
Jun 28, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ormond Beach, FL (United States)

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