FDA Inspection 677578 — Carter BloodCare at Hulen

Carter BloodCare at Hulen — FEI 3000719944

The FDA completed an inspection of Carter BloodCare at Hulen on August 30, 2010 in Fort Worth, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 30, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)

Citations

IDCFRDescription
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
8821 CFR 606.100(b)(9)Written methods for investigating adverse reactions