FDA Inspection 811092 — OneBlood, Inc.

OneBlood, Inc. — FEI 1077496

The FDA completed an inspection of OneBlood, Inc. on December 14, 2012 in Fort Lauderdale, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 14, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Lauderdale, FL (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report
9821 CFR 606.100(c)Thorough investigations