Intercos Europe SpA 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 3005291719.
Intercos Europe SpA
Dovera, -, Italy
Issue DateJune 24, 2016
FEI Number3005291719
CountryItaly
Status
No Warning LetterProduct Type
Drugs