# Stryker Corporation – FDA Inspection, Jun 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/stryker-corporation/f25e380b-2138-4f26-b3b2-360f04e543dc
Source feed: FDA_Inspections

> FDA inspection 791489 of Stryker Corporation, June 18, 2012. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791489
- Company Name: Stryker Corporation
- Inspection Date: 2012-06-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- [FDA Inspection 806763 - 2012-11-09](https://www.keypedia.com/records/fda_inspections/stryker-corporation/a59a9ed7-bc6d-48f7-ba09-1d1578579776)
- [FDA Inspection 682479 - 2010-09-24](https://www.keypedia.com/records/fda_inspections/stryker-corporation/85948abf-5435-4a05-abb1-ae55467dfbd8)
- [FDA Inspection 583137 - 2009-05-14](https://www.keypedia.com/records/fda_inspections/stryker-corporation/69d21025-1eec-4c2d-8630-92ab1538a1ad)

Company: https://www.keypedia.com/companies/stryker-corporation/f5cfb79a-98da-4227-9c0f-fd9a0294bcbb

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