FDA inspection

Medela Inc: FDA inspection ending Jan 24, 2000

FDA inspection 10911 · Voluntary Action Indicated (VAI) · McHenry, IL

Key facts

Inspection ID 10911
Firm Medela Inc
FEI number 1419937
Address 1101 Corporate Dr
City McHenry
State IL
ZIP 60050-7006
Fiscal year 2000
Inspection end date Jan 24, 2000
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
  • 10–99 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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