DashboardForm 483sForm 483 Details

AMTRION GMBH (Formerly Haseke & Kroemker) 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 3005285078.

AMTRION GMBH (Formerly Haseke & Kroemker)

Porta Westfalica, -, Germany
Issue DateApril 06, 2018
FEI Number3005285078
CountryGermany
Status
No Warning Letter
Product Type
Devices
AMTRION GMBH (Formerly Haseke & Kroemker) FDA Form 483, Porta Westfalica, April 6, 2018