FDA inspection

Q-Med AB: FDA inspection ending Jan 29, 2009

FDA inspection 567005 · Voluntary Action Indicated (VAI) · Uppsala

Key facts

Inspection ID 567005
Firm Q-Med AB
FEI number 3003347293
Address Seminariegatan 31
City Uppsala
Country Sweden
Fiscal year 2009
Inspection end date Jan 29, 2009
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

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
  • 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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