# Smith & Nephew, Inc. – FDA Inspection, Dec 8, 2015

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

> FDA inspection 960574 of Smith & Nephew, Inc., December 08, 2015. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1015137 - 2017-05-25
- [FDA Inspection 740641 - 2011-08-15](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/222e3ce1-d872-459f-90fc-18018f5755df)

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