Arjo Dominican Republic 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 3012292104.
Arjo Dominican Republic
Itabo, Haina, Dominican Republic (the)
Issue DateMay 28, 2026
FEI Number3012292104
CountryDominican Republic (the)
Status
No Warning LetterProduct Type
Devices