FDA Inspection 1018250 — Coastal Bend Blood Center

Coastal Bend Blood Center — FEI 1671283

The FDA completed an inspection of Coastal Bend Blood Center on July 14, 2017 in Corpus Christi, 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
July 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Corpus Christi, TX (United States)

Citations

IDCFRDescription
1503021 CFR 606.60(b)Equipment calibration frequency