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FDA Inspection
•Stryker Neurovascular, Inc.•December 2, 2015

Stryker Neurovascular, Inc. – FDA Inspection, Dec 2, 2015

Record Details

This FDA Inspection record concerns Stryker Neurovascular, Inc., with an inspection on December 2, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Stryker Neurovascular, Inc.
Inspection Date
December 2, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 107ad27b-6bdf-4762-b21b-fa589aa6913c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
956410
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Stryker Neurovascular, Inc.

4
DateClassificationOfficeProject area
May 3, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
January 18, 2018Not classifiedDenver District Office
November 1, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 2, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Stryker Neurovascular, Inc.
  • FDA Inspection 1229210 - 2024-05-03
  • FDA Inspection 1039088 - 2018-01-18
  • FDA Inspection 805526 - 2012-11-01
  • FDA Inspection 561509 - 2009-02-02

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