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FDA Inspection
•Carter BloodCare•August 25, 2017

Carter BloodCare – FDA Inspection, Aug 25, 2017

Record Details

This FDA Inspection record concerns Carter BloodCare, with an inspection on August 25, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Carter BloodCare
Inspection Date
August 25, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Decarlos A. Gomez (Issuing Officer)
View Company Profile

ID · 7c649d44-390b-4689-b634-469600b3fd89

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1023814
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Carter BloodCare

5
DateClassificationOfficeProject area
July 21, 2026Not classifiedDallas District Office
May 23, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 10, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 13, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 13, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Carter BloodCare
  • FDA Inspection 1329542 - 2026-07-21
  • FDA Inspection 1092617 - 2019-05-23
  • FDA Inspection 938894 - 2015-07-10
  • FDA Inspection 818232 - 2013-02-13
  • FDA Inspection 706855 - 2011-01-13

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