# Smith & Nephew, Inc. Advanced Surgical Devices Division, Oklahoma City, OK – FDA Inspections

Source: https://www.keypedia.com/companies/smith-nephew-inc-advanced-surgical-devices-division/ddde9862-4771-42a1-b99b-9539c555778d

> Inspection records and compliance data for Smith & Nephew, Inc. Advanced Surgical Devices Division in Oklahoma City, Oklahoma. 3 FDA inspections on record, last inspected August 21, 2017.

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## Details

- Name: Smith & Nephew, Inc. Advanced Surgical Devices Division
- FEI Number: 1643264
- Address Line 1: 76 S Meridian Ave
- City: Oklahoma City
- State: Oklahoma
- Zip Code: 73107
- Country Name: United States
- Address: 76 S Meridian Ave, Oklahoma City, Oklahoma 73107, United States
- Country: United States

## Related Documents

- FDA Inspection 1031107 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2017-08-21 — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2017
- FDA Inspection 1031107 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2017-08-21 — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2017
- [FDA Inspection 834988 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2013-06-11](https://www.keypedia.com/records/fda_inspections/smith-nephew-inc-advanced-surgical-devices-division/90162397-f040-4398-9683-a0b5cc66706a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2013
- FDA Inspection 834988 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2013-06-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2013
- FDA Inspection 601510 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2009-07-31 — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2009
- FDA Inspection 601510 - Smith & Nephew, Inc. Advanced Surgical Devices Division - 2009-07-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2009

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