FDA inspection

Octapharma Plasma, Inc.: FDA inspection ending Mar 28, 2009

FDA inspection 573577 · Voluntary Action Indicated (VAI) · Terre Haute, IN

Key facts

Inspection ID 573577
Firm Octapharma Plasma, Inc.
FEI number 3007198422
Address 115 Walnut St
City Terre Haute
State IN
ZIP 47807
Country United States
Fiscal year 2009
Inspection end date Mar 28, 2009
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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