FDA Inspection 1276506 — HemaTerra Technolgies LLC

HemaTerra Technolgies LLC — FEI 3015108978

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