# FDA Inspection 909000 - Stryker Puerto Rico, LLC - November 14, 2014

Source: https://www.keypedia.com/records/fda_inspections/stryker-puerto-rico-llc/6fefb661-d3e6-4de1-8ed2-18ab2d2ccc76
Source feed: FDA_Inspections

> FDA Inspection 909000 for Stryker Puerto Rico, LLC on November 14, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909000
- Company Name: Stryker Puerto Rico, LLC
- Inspection Date: 2014-11-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/stryker-puerto-rico-llc/15ef9e21-ef4c-473e-af65-f2cd3b7cc07f

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