FDA inspection

Isopure Corp.: FDA inspection ending Aug 25, 2011

FDA inspection 741461 · Voluntary Action Indicated (VAI) · Louisville, KY

Key facts

Inspection ID 741461
Firm Isopure Corp.
FEI number 3013942511
Address 11851 Plantside Dr
City Louisville
State KY
ZIP 40299
Country United States
Fiscal year 2011
Inspection end date Aug 25, 2011
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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