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FDA Inspection
•Stryker Corporation•August 25, 2016

Stryker Corporation – FDA Inspection, Aug 25, 2016

Record Details

This FDA Inspection record concerns Stryker Corporation, with an inspection on August 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Stryker Corporation
Inspection Date
August 25, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fb435a32-58b6-44ee-ae49-a81e9525d4ea

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
981779
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Stryker Corporation

7
DateClassificationOfficeProject area
November 21, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 25, 2018Not classifiedSan Francisco District Office
September 18, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
October 8, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
March 14, 2012VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 7 other inspections on the company page
Other documents for Stryker Corporation
  • FDA Inspection 1110636 - 2019-11-21
  • FDA Inspection 1077335 - 2018-05-25
  • FDA Inspection 943626 - 2015-09-18
  • FDA Inspection 896766 - 2014-10-08
  • FDA Inspection 772257 - 2012-03-14

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