Dio Corporation 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 3007126709.
Dio Corporation
Haeundae, -, Korea (the Republic of)
Issue DateFebruary 11, 2010
FEI Number3007126709
CountryKorea (the Republic of)
Status
No Warning LetterProduct Type
Devices