CURALLUX LLC

Form 483

Doral, Florida, United StatesFEI 3010123655Issued May 16, 2013

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 3010123655.

Observations16

Issue DateMay 16, 2013

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: CURALLUX LLC
Location: Doral, Florida, United States
FEI Number: 3010123655
Product Type: Devices
Issue Date: May 16, 2013
Country: United States

Inspection History, 2013 to 2019

NAI1

VAI1

OAI2

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

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CURALLUX LLC FDA Form 483, Doral, Florida, May 16, 2013