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FDA Inspection
•Stryker Leibinger GmbH & Co. KG•July 27, 2017

Stryker Leibinger GmbH & Co. KG – FDA Inspection, Jul 27, 2017

Record Details

This FDA Inspection record concerns Stryker Leibinger GmbH & Co. KG, with an inspection on July 27, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Stryker Leibinger GmbH & Co. KG
Inspection Date
July 27, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Thomas E. Friel (FDA Associated Person)
View Company Profile

ID · 61601172-2f85-49d8-8ee2-57e6b40acf8b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1032071
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Stryker Leibinger GmbH & Co. KG

2
DateClassificationOfficeProject area
February 27, 2025NAIPostmarket Assurance: Devices
November 14, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Stryker Leibinger GmbH & Co. KG
  • FDA Inspection 1264818 - 2025-02-27
  • FDA Inspection 856404 - 2013-11-14

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