Bernstein AG

Form 483

Porta Westfalica, -, GermanyFEI 3003635889Issued February 26, 2009

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 3003635889.

Observations3

Issue DateFebruary 26, 2009

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Bernstein AG
Location: Porta Westfalica, -, Germany
FEI Number: 3003635889
Product Type: Devices
Issue Date: February 26, 2009
Country: Germany

Inspection History, 2009 to 2016

NAI1

VAI1

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

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Bernstein AG FDA Form 483, Porta Westfalica, February 26, 2009