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FDA Inspection 604811 — Carter BloodCare

Carter BloodCare — FEI 3002603147

The FDA completed an inspection of Carter BloodCare on August 17, 2009 in Bedford, 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
August 17, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bedford, TX (United States)

Facility

Other inspections at this facility

  • 1217918 (NAI Tue Aug 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1093449 (NAI Fri Apr 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1033975 (VAI Wed Dec 06 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 846717 (NAI Thu Aug 29 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 736481 (VAI Wed Jul 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources