QIAGEN Instruments 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 3005621256.
QIAGEN Instruments AG
Hombrechtikon, -, Switzerland
Issue DateJuly 19, 2013
FEI Number3005621256
CountrySwitzerland
Status
No Warning LetterProduct Type
Devices