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Dufner Instrumente 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 3002806862.

Dufner Instrumente GmbH

Tuttlingen, -, Germany
Issue DateJune 25, 2015
FEI Number3002806862
CountryGermany
Status
No Warning Letter
Product Type
Devices
Dufner Instrumente GmbH FDA Form 483, Tuttlingen, June 25, 2015