FDA inspection

Microlife Medical Home Solutions, Inc.: FDA inspection ending Jan 17, 2003

FDA inspection 254840 · Voluntary Action Indicated (VAI) · Golden, CO

Key facts

Inspection ID 254840
Firm Microlife Medical Home Solutions, Inc.
FEI number 3003288989
Address 2801 Youngfield St Ste 241
City Golden
State CO
ZIP 80401-0208
Fiscal year 2003
Inspection end date Jan 17, 2003
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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