# FDA Inspection 993232 - Smith & Nephew Inc. - November 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/b6ce174c-1399-4225-aeeb-107610fd0551
Source feed: FDA_Inspections

> FDA Inspection 993232 for Smith & Nephew Inc. on November 09, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993232
- Company Name: Smith & Nephew Inc.
- Inspection Date: 2016-11-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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