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FDA Inspection 591532 — Coastal Bend Blood Center

Coastal Bend Blood Center — FEI 1671283

The FDA completed an inspection of Coastal Bend Blood Center on June 8, 2009 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). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 8, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Corpus Christi, TX (United States)

Facility

Other inspections at this facility

  • 1266889 (NAI Fri Mar 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1097872 (NAI Thu Jun 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018250 (VAI Fri Jul 14 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 930894 (NAI Wed Jun 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 829012 (NAI Fri Apr 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources