FDA Inspection 963720 — Carter BloodCare

Carter BloodCare — FEI 3000204655

The FDA completed an inspection of Carter BloodCare on Jan 13, 2016 in Rockwall, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 13, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rockwall, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.