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FDA Inspection 983201 — Carter Bloodcare - Denton

Carter Bloodcare - Denton — FEI 3004853345

The FDA completed an inspection of Carter Bloodcare - Denton on August 15, 2016 in Denton, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 15, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Denton, TX (United States)

Facility

Other inspections at this facility

  • 1210113 (NAI Thu Jun 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066196 (NAI Wed Sep 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891629 (NAI Wed Jul 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 799644 (NAI Thu Sep 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 675928 (NAI Thu Aug 12 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources