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Teleflex Medical Tuttlingen 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 3010089057.

Teleflex Medical Tuttlingen GmbH

Wurmlingen, -, Germany
Issue DateNovember 05, 2013
FEI Number3010089057
CountryGermany
Status
No Warning Letter
Product Type
Devices
Teleflex Medical Tuttlingen GmbH FDA Form 483, Wurmlingen, November 5, 2013