# Smith & Nephew, Inc. – FDA Inspection, Aug 2, 2017

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

> FDA inspection 1020184 of Smith & Nephew, Inc., August 02, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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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)
- 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: 3

## Related Documents

- [FDA Inspection 1158635 - 2021-12-09](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc/8213783d-e23a-4a05-8e34-dd93ec601e1b)
- FDA Inspection 1041637 - 2018-02-02
- FDA Inspection 1012033 - 2017-05-11
- FDA Inspection 984209 - 2016-08-17
- FDA Inspection 885233 - 2014-06-27

## Related Officers

- Issuing Officer
- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

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

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