# FDA Inspection 601510 - Smith & Nephew, Inc. Advanced Surgical Devices Division - July 31, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-inc-advanced-surgical-devices-division/fd28df17-7015-46d4-a61f-1bd86508dba6/
Source feed: FDA_Inspections

> FDA Inspection 601510 for Smith & Nephew, Inc. Advanced Surgical Devices Division on July 31, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601510
- Company Name: Smith & Nephew, Inc. Advanced Surgical Devices Division
- Inspection Date: 2009-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 601510 - 2009-07-31](https://www.globalkeysolutions.net/api/records/fda_inspections/smith-nephew-inc-advanced-surgical-devices-division/75571f3e-d653-4500-b15e-098977e212b4/)

Company: https://www.globalkeysolutions.net/companies/smith-nephew-inc-advanced-surgical-devices-division/ddde9862-4771-42a1-b99b-9539c555778d

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