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Stryker GmbH, Selzach, Switzerland – FDA Inspections

Inspection records and compliance data for Stryker GmbH in Selzach. 4 FDA inspections on record, 1 Form 483, last inspected March 27, 2025.

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Company Profile

This profile covers Stryker GmbH based in Selzach, Switzerland.

FDA Inspection History

FDA inspections
4
OAI
0
VAI
2
NAI
2
Form 483s
1
Warning letters
0

First inspected November 6, 2008. Last inspected March 27, 2025.

Most cited issue areas

  • Lack of or inadequate procedures1 inspection

FDA inspections (4)

DateResultFDA center(s)Insp. #
March 27, 2025NAIMedical Devices & Rad Health · Postmarket Assurance: Medical Devices1263754
February 25, 2016VAIMedical Devices & Rad Health · Compliance: Devices965787
September 22, 2011NAIMedical Devices & Rad Health · Compliance: Devices750625
November 6, 2008VAIMedical Devices & Rad Health · Compliance: Devices551172
FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

Belimed AG
Hocoma AG
JABIL SWITZERLAND MANUFACTURING GMBH (Bettlach)
Unisensor AG
Bracco Injeneering S.A.
Reha Technology Ag
Smith & Nephew Orthopaedics AG
GETSET SURGICAL SA
Cellpack Ag
Medicoat AG
Company Information

Name

Stryker GmbH

FEI Number

3002807830

Address

Bohnackerweg 1, Selzach, Switzerland

Country

Switzerland

ID: c74b50c4-3566-425d-9331-7fb21b736586

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