FDA inspection

HemaTerra Technolgies LLC: FDA inspection ending Jul 10, 2025

FDA inspection 1276506 · No Action Indicated (NAI) · Baltimore, MD

Key facts

Inspection ID 1276506
Firm HemaTerra Technolgies LLC
FEI number 3015108978
Address 180 W Ostend St Ste 267a
City Baltimore
State MD
ZIP 21230
Country United States
Fiscal year 2025
Inspection end date Jul 10, 2025
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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