FDA Inspection 778151 — OneBlood, Inc.

OneBlood, Inc. — FEI 1033367

The FDA completed an inspection of OneBlood, Inc. on Apr 23, 2012 in Port Charlotte, 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
Apr 23, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Port Charlotte, FL (United States)

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