Delcon Srl Form 483 Details

Form 483

Source: FDA, document on fileFDA released the Form 483 itself and the document linked above is FDA's own file, served from fda.gov.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3014345398.

Delcon Srl

Issue DateMarch 24, 2023

FEI Number3014345398

CountryN/A

Status

No Warning Letter

Establishment Type

Medical Device Manufacturer