DashboardForm 483sForm 483 Details

Kleinmontagen Wiechmann GmbH Form 483 Details

Form 483
View FDA's record for this firm
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 3009938288.

Kleinmontagen Wiechmann GmbH

Grabow, -, Germany
Issue DateJanuary 30, 2013
FEI Number3009938288
CountryGermany
Status
No Warning Letter
Product Type
Devices
Kleinmontagen Wiechmann GmbH FDA Form 483, Grabow, January 30, 2013