# FDA Inspection 1110636 - Stryker Corporation - November 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/stryker-corporation/d5ef1dc5-edd3-4dda-aff5-dc0413adb8a6
Source feed: FDA_Inspections

> FDA Inspection 1110636 for Stryker Corporation on November 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110636
- Company Name: Stryker Corporation
- Inspection Date: 2019-11-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1110636 - 2019-11-21](https://www.keypedia.com/records/fda_inspections/stryker-corporation/76a21ad0-9c6c-47e6-820c-c344922fd02e)
- [FDA Inspection 981779 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/stryker-corporation/fb435a32-58b6-44ee-ae49-a81e9525d4ea)
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- [FDA Inspection 981779 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/stryker-corporation/68505d05-1477-4922-9614-4bad3986cda4)
- [FDA Inspection 943626 - 2015-09-18](https://www.keypedia.com/records/fda_inspections/stryker-corporation/3919eeca-6998-48e2-a76f-b8793f361acd)

Company: https://www.keypedia.com/companies/stryker-corporation/5d1b3e70-5dcc-4966-b0ea-0c4a31acbf43

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7