Medtronic CryoCath LP

Form 483

Montreal, -, CanadaFEI 3002648230Issued December 10, 2009

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3002648230.

Observations1

Issue DateDecember 10, 2009

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Medtronic CryoCath LP
Location: Montreal, -, Canada
FEI Number: 3002648230
Product Type: Devices
Issue Date: December 10, 2009
Country: Canada

Inspection History, 2009 to 2024

NAI2

VAI3

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

Act on This Form 483

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Medtronic CryoCath LP FDA Form 483, Montreal, December 10, 2009