Diasorin Deutschland GmbH 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 3004434309.
Diasorin Deutschland GmbH
Dietzenbach, -, Germany
Issue DateMay 30, 2014
FEI Number3004434309
CountryGermany
Status
No Warning LetterProduct Type
Devices