# FDA Inspection 960574 - Smith & Nephew, Inc. - December 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/791e03db-6cce-48d8-a22c-c05906e33dd0
Source feed: FDA_Inspections

> FDA Inspection 960574 for Smith & Nephew, Inc. on December 08, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960574
- Company Name: Smith & Nephew, Inc.
- Inspection Date: 2015-12-08
- Classification: Voluntary Action Indicated (VAI)
- 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/smith-nephew-inc/000fa36f-a97a-49b7-8a63-1a5c135e6f31

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