Smith & Nephew, Inc. Advanced Surgical Devices Division

Form 483

Oklahoma City, Oklahoma, United StatesFEI 1643264Issued July 31, 2009

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1643264.

Observations2

Issue DateJuly 31, 2009

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Smith & Nephew, Inc. Advanced Surgical Devices Division
Location: Oklahoma City, Oklahoma, United States
FEI Number: 1643264
Product Type: Devices
Issue Date: July 31, 2009
Country: United States

Inspection History, 2009 to 2017

NAI1

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Smith & Nephew, Inc. Advanced Surgical Devices Division FDA Form 483, Oklahoma City, Oklahoma, July 31, 2009