FDA inspection

Dura Medical Equipment: FDA inspection ending Aug 24, 2010

FDA inspection 678263 · Voluntary Action Indicated (VAI) · Miami Lakes, FL

Key facts

Inspection ID 678263
Firm Dura Medical Equipment
FEI number 1000143687
Address 7835 NW 148th St
City Miami Lakes
State FL
ZIP 33016
Country United States
Fiscal year 2010
Inspection end date Aug 24, 2010
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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