FDA inspection

Covidien, LLC: FDA inspection ending Jan 9, 2007

FDA inspection 455490 · Voluntary Action Indicated (VAI) · Minneapolis, MN

Key facts

Inspection ID 455490
Firm Covidien, LLC
FEI number 3004962788
Address 161 Cheshire Ln N Ste 100
City Minneapolis
State MN
ZIP 55441-5433
Fiscal year 2007
Inspection end date Jan 9, 2007
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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