MeKo Manufacturing e.K.

Form 483FOIA Uncovered

Sarstedt, -, GermanyFEI 3009937642Issued February 21, 2019

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 3009937642.

Observations2

Issue DateFebruary 21, 2019

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: MeKo Manufacturing e.K.
Location: Sarstedt, -, Germany
FEI Number: 3009937642
Product Type: Devices
Issue Date: February 21, 2019
Country: Germany

Inspection History, 2016 to 2019

NAI1

VAI1

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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MeKo Manufacturing e.K. FDA Form 483, Sarstedt, February 21, 2019