FDA inspection

Medtronic AVE: FDA inspection ending Sep 19, 2002

FDA inspection 238528 · Official Action Indicated (OAI) · Sunrise, FL

Key facts

Inspection ID 238528
Firm Medtronic AVE
FEI number 1051676
Address 799 International Pkwy
City Sunrise
State FL
ZIP 33325-6220
Fiscal year 2002
Inspection end date Sep 19, 2002
Classification Official Action Indicated (OAI)
Project area Product Evaluation: Med Devices
Product type Devices

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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