# FDA Inspection 606855 - Smith & Nephew Inc. - August 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/685a52fd-4d6a-4d7b-afb7-58a1979d77e5
Source feed: FDA_Inspections

> FDA Inspection 606855 for Smith & Nephew Inc. on August 06, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 606855
- Company Name: Smith & Nephew Inc.
- Inspection Date: 2009-08-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1155885 - 2021-10-26](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/80a77c2d-c193-43ed-88e2-141037392fd9)
- [FDA Inspection 993232 - 2016-11-09](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/b6ce174c-1399-4225-aeeb-107610fd0551)
- [FDA Inspection 920985 - 2015-03-26](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/358cc24b-160a-4dab-9742-f5bbf7a0698a)
- [FDA Inspection 920985 - 2015-03-26](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/0c127ce5-7ad1-4ced-a330-5d812b30f2a3)
- [FDA Inspection 606855 - 2009-08-06](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/d0058292-fab6-484a-a365-07fc2b0884fe)

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