Elexxion AG Form 483 Details
Form 483Source: 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 3005228795.
Elexxion AG
Radolfzell am Bodensee, -, Germany
Issue DateFebruary 16, 2012
FEI Number3005228795
CountryGermany
Status
No Warning LetterProduct Type
Devices