Remel Europe Ltd.

Form 483

Dartford, -, United KingdomFEI 3003750284Issued May 31, 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 3003750284.

Observations3

Issue DateMay 31, 2013

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Remel Europe Ltd.
Location: Dartford, -, United Kingdom
FEI Number: 3003750284
Product Type: Devices
Issue Date: May 31, 2013
Country: United Kingdom

Inspection History, 2009 to 2016

NAI1

VAI1

OAI1

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

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Remel Europe Ltd. FDA Form 483, Dartford, May 31, 2013