FDA Inspection 1276506 — HemaTerra Technolgies LLC

HemaTerra Technolgies LLC — FEI 3015108978

The FDA completed an inspection of HemaTerra Technolgies LLC on Jul 10, 2025 in Baltimore, MD. 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
Jul 10, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Baltimore, MD (United States)

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