Smith & Nephew Inc.

Form 483

Andover, Massachusetts, United StatesFEI 3003604053Issued August 06, 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 3003604053.

Observations2

Issue DateAugust 06, 2009

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Smith & Nephew Inc.
Location: Andover, Massachusetts, United States
FEI Number: 3003604053
Product Type: Devices
Issue Date: August 06, 2009
Country: United States

Inspection History, 2009 to 2021

NAI2

VAI1

OAI1

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

Act on This Form 483

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Smith & Nephew Inc. FDA Form 483, Andover, Massachusetts, August 6, 2009