EyeKon Medical, Inc.

Form 483

Clearwater, Florida, United StatesFEI 1038833Issued February 16, 2018

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 1038833.

Observations7

Issue DateFebruary 16, 2018

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: EyeKon Medical, Inc.
Location: Clearwater, Florida, United States
FEI Number: 1038833
Product Type: Devices
Issue Date: February 16, 2018
Country: United States

Inspection History, 2008 to 2025

NAI1

VAI3

OAI1

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

Act on This Form 483

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EyeKon Medical, Inc. FDA Form 483, Clearwater, Florida, February 16, 2018