Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse)

FDA inspection history in Ravensburg, Germany, 2010 to 2024

5
Form 483s

Every document, by year

  • Form 483

2010: one Form 483; 2017: one Form 483; 2019: one Form 483; 2022: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2010One Form 483, at Ravensburg, Germany.
  2. 2010The longest 483 on file: 9 observations over 3 pages at Ravensburg, Germany.
  3. 2017–19Two Form 483s, at Ravensburg, Germany.
  4. 2022–24Two Form 483s, at Ravensburg, Germany.

Cited most

Across all Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) observations on file

The complete Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) file.

All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$421$495

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Sites

Documents

5 on file, newest first
DateDocumentPrice
2024-09-20483 Form 483$99
2022-08-19483 Form 483$99
2019-05-17483 Form 483$99
2017-01-17483 Form 483$99
2010-04-01483 Form 483$99

FEI number 3002270322 · most recent document Sep 20, 2024

About Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse)

How many FDA Form 483s has Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) received?

FDA Intel has 5 Form 483s on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse); the most recent is dated Sep 20, 2024.

When was Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) last inspected by FDA?

The most recent FDA inspection document on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) is a Form 483 dated Sep 20, 2024, for the site in Ravensburg, Germany.

What did FDA cite at Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse)?

The regulations cited most in the observations on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) are 21 CFR 211.113 (Control of microbiological contamination), 4 times; 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.198 (Complaint files), 3 times.