Sanofi-Aventis Deutschland GmbH

FDA inspection history in Frankfurt am Main, Germany, 2012 to 2025

1
Form 483
1
Close-out

Every document, by year

  • Form 483
  • Close-out

2012: one close-out letter; 2025: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2012One close-out letter, at Frankfurt am Main, Germany.
  2. 2025One Form 483, at Frankfurt am Main, Germany.

Cited most

Across all Sanofi-Aventis Deutschland observations on file

The complete Sanofi-Aventis Deutschland file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2025-01-16483 Form 483$99
2012-08-14Close-out Close-out letter$99

FEI number 3003195501 · most recent document Jan 16, 2025

About Sanofi-Aventis Deutschland GmbH

How many FDA Form 483s has Sanofi-Aventis Deutschland GmbH received?

FDA Intel has 1 Form 483 on file for Sanofi-Aventis Deutschland GmbH; the most recent is dated Jan 16, 2025.

When was Sanofi-Aventis Deutschland GmbH last inspected by FDA?

The most recent FDA inspection document on file for Sanofi-Aventis Deutschland GmbH is a Form 483 dated Jan 16, 2025, for the site in Frankfurt am Main, Germany.

What did FDA cite at Sanofi-Aventis Deutschland GmbH?

The regulations cited most in the observations on file for Sanofi-Aventis Deutschland GmbH are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.