FDA inspection

Q-Med AB: FDA inspection ending Aug 24, 2017

FDA inspection 1025913 · No Action Indicated (NAI) · Uppsala

Key facts

Inspection ID 1025913
Firm Q-Med AB
FEI number 3003347293
Address Seminariegatan 21
City Uppsala
Country Sweden
Fiscal year 2017
Inspection end date Aug 24, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections