FDA Inspection 594217 — Carter BloodCare at Keller

Carter BloodCare at Keller — FEI 3003706080

The FDA completed an inspection of Carter BloodCare at Keller on June 24, 2009 in Keller, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 24, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Keller, TX (United States)

Citations

IDCFRDescription
16021 CFR 606.160(a)(1)Person performing, test results, interpretation