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Smith & Nephew Orthopaedics GmbH Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed 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 this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3002465897.

Smith & Nephew Orthopaedics GmbH

Tuttlingen, -, Germany
Issue DateMay 07, 2015
FEI Number3002465897
CountryGermany
Status
No Warning Letter
Product Type
Devices
Smith & Nephew Orthopaedics GmbH FDA Form 483, Tuttlingen, May 7, 2015