Boston Scientific Corporation

Form 483

Issued to: Guidant Corporation

Saint Paul, Minnesota, United StatesFEI 2124215Issued July 11, 2015

View Form 483 PDF

Source: FDA, document on file. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2124215.

Observations1

Issue DateJuly 11, 2015

StatusNo Warning Letter

Establishment TypeMedical Device Manufacturer

Related Inspections10

Establishment Details

Firm: Boston Scientific Corporation
Issued To: Guidant Corporation
Location: Saint Paul, Minnesota, United States
FEI Number: 2124215
Establishment Type: Medical Device Manufacturer
Product Type: Devices
Issue Date: July 11, 2015
Country: United States

Inspection History, 2013 to 2025

NAI7

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Boston Scientific Corporation FDA Form 483, Saint Paul, Minnesota, July 11, 2015