Iradimed Corporation

Form 483

orlando, Florida, United StatesFEI 3005053560Issued July 18, 2016

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 3005053560.

Observations3

Issue DateJuly 18, 2016

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Iradimed Corporation
Location: orlando, Florida, United States
FEI Number: 3005053560
Product Type: Devices
Issue Date: July 18, 2016
Country: United States

Inspection History, 2010 to 2019

VAI3

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Iradimed Corporation FDA Form 483, orlando, Florida, July 18, 2016