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Q-Med AB, Uppsala, Sweden – FDA Inspections

Inspection records and compliance data for Q-Med AB in Uppsala. 8 FDA inspections on record (1 OAI), 1 Form 483, last inspected March 27, 2026.

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Company Profile

This profile covers Q-Med AB based in Uppsala, Sweden.

FDA Inspection History

FDA inspections
8
OAI
1
VAI
1
NAI
5
Unclassified
1
Form 483s
1
Warning letters
0

First inspected January 29, 2009. Last inspected March 27, 2026.

FDA inspections (8)

DateResultFDA center(s)Insp. #
March 27, 2026Not classifiedHuman Drugs1313816
January 19, 2023NAIMedical Devices & Rad Health · Bioresearch Monitoring1199979
March 29, 2018NAIMedical Devices & Rad Health · Postmarket Assurance: Devices1048550
August 24, 2017NAIMedical Devices & Rad Health · Postmarket Assurance: Devices1025913
February 13, 2015NAIMedical Devices & Rad Health · Postmarket Assurance: Devices921654
June 21, 2012NAIMedical Devices & Rad Health · Bioresearch Monitoring789285
July 9, 2010OAIMedical Devices & Rad Health · Compliance: Devices678939
January 29, 2009VAIMedical Devices & Rad Health · Postmarket Assurance: Devices564695
FDA documents

Form 483s (1)

  • Form 483s · March 27, 2026
People (2)
Jun Liu
Person
Qibing Zhou
Person
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Sunbeam Products, Inc.
DiaPharma Group Inc
Bausch Health Americas, Inc.
Company Information

Name

Q-Med AB

FEI Number

3003347293

Address

Seminariegatan 21, Uppsala, Sweden

Country

Sweden

ID: 032a27fc-d1ee-4ed3-98da-38090c026849

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