Boston Scientific Corporation Form 483 Details

Form 483

Issued to: Guidant Corporation

Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 2124215.

Boston Scientific Corporation

Saint Paul, Minnesota, United States

Issue DateJuly 11, 2015

FEI Number2124215

CountryUnited States

Status

No Warning Letter

Product Type

Devices

Establishment Type

Medical Device Manufacturer