# FDA Inspection 1020184 - Smith & Nephew, Inc. - August 02, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/smith-nephew-inc/fd39576a-b8ba-4bf3-b687-8febeb19e56d/
Source feed: FDA_Inspections

> FDA Inspection 1020184 for Smith & Nephew, Inc. on August 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020184
- Company Name: Smith & Nephew, Inc.
- Inspection Date: 2017-08-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/smith-nephew-inc/fc8c02e8-e978-443f-b02c-41a49b88ca49

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