Meditech KFT

Form 483

Budapest, -, HungaryFEI 3003764019Issued April 13, 2012

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 3003764019.

Observations9

Issue DateApril 13, 2012

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Meditech KFT
Location: Budapest, -, Hungary
FEI Number: 3003764019
Product Type: Devices
Issue Date: April 13, 2012
Country: Hungary

Inspection History, 2012 to 2018

VAI2

OAI1

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

Act on This Form 483

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Meditech KFT FDA Form 483, Budapest, April 13, 2012