Eurofins BioPharma Product Testing Czech Republic s.r.o. 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 3008920466.
Eurofins BioPharma Product Testing Czech Republic s.r.o.
Brno-Jih, -, Czech Republic
Issue DateJuly 29, 2014
FEI Number3008920466
CountryCzech Republic
Status
No Warning LetterProduct Type
Drugs