Sanofi-Aventis Deutschland GmbH

Form 483

Frankfurt Am Main, -, GermanyFEI 3003195501Issued December 10, 2015

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 3003195501.

Observations1

Issue DateDecember 10, 2015

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Sanofi-Aventis Deutschland GmbH
Location: Frankfurt Am Main, -, Germany
FEI Number: 3003195501
Product Type: Devices
Issue Date: December 10, 2015
Country: Germany

Inspection History, 2010 to 2022

NAI3

VAI6

OAI1

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

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Sanofi-Aventis Deutschland GmbH FDA Form 483, Frankfurt Am Main, December 10, 2015