Diasol, Inc Form 483 Details
Form 483Source: FDA record for this establishmentFDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3007137482.
Diasol, Inc
Phoenix, Arizona, United States
Issue DateFebruary 03, 2010
FEI Number3007137482
CountryUnited States
Status
1 Related Warning LetterProduct Type
Devices