# Smith & Nephew, Inc. – FDA Inspection, Aug 31, 2011

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/ada4f439-bd7d-4cbc-a929-61cc75c8a4b9
Source feed: FDA_Inspections

> FDA inspection 743018 of Smith & Nephew, Inc., August 31, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 743018
- Company Name: Smith & Nephew, Inc.
- Inspection Date: 2011-08-31
- 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 907062 - 2015-01-13
- [FDA Inspection 858923 - 2013-11-26](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/3e04d3e2-68f8-4f4d-b510-bcf42aa146d3)
- FDA Inspection 610762 - 2009-09-04

Company: https://www.keypedia.com/companies/smith-nephew-inc/e0dd5fec-72a6-4e0a-9b58-e213b7e0c570

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