# Smith & Nephew Inc. – FDA Inspection, Aug 6, 2009

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/d0058292-fab6-484a-a365-07fc2b0884fe
Source feed: FDA_Inspections

> FDA inspection 606855 of Smith & Nephew Inc., August 06, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 606855
- Company Name: Smith & Nephew Inc.
- Inspection Date: 2009-08-06
- 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: 2

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- [FDA Inspection 920985 - 2015-03-26](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/358cc24b-160a-4dab-9742-f5bbf7a0698a)

Company: https://www.keypedia.com/companies/smith-nephew-inc/c5968aab-275e-41cd-b545-a7c3853119aa

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