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Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Latest inspection VAI · Jul 21, 2023
No warning letters matched by name

Inspections 10

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)" is on file.

What these totals cover: FDA records filed under the name "Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)" and its spelling variant "Vetter Pharma Fertigung Gmbh And Co. Kg (Ravensburg Mooswiesen)".

Latest inspection: Jul 21, 2023 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	0	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	10	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen): FDA inspections per year

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	0	0	0	0
2024	0	0	0	0	0
2023	2	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	1	0	0	0	0
2019	0	0	0	0	0
2018	1	0	0	0	0
2017	1	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent FDA inspections

10 inspections from Apr 1, 2010 to Jul 21, 2023.

Date	Site	Product	Classification	FEI
Jul 21, 2023	Ravensburg, Germany	Drugs	Voluntary Action Indicated (VAI)	3005987757
Apr 19, 2023	Ravensburg, Germany	Devices	No Action Indicated (NAI)	3005987757
Jul 20, 2020	Ravensburg, Germany	Drugs	Voluntary Action Indicated (VAI)	3005987757
Jun 12, 2018	Ravensburg, Germany	Drugs	No Action Indicated (NAI)	3005987757
Nov 2, 2017	Ravensburg, Germany	Biologics	Voluntary Action Indicated (VAI)	3005987757
Jul 26, 2016	Ravensburg, Germany	Drugs	No Action Indicated (NAI)	3005987757
Dec 5, 2014	Ravensburg, Germany	Drugs	Voluntary Action Indicated (VAI)	3005987757
Oct 28, 2013	Ravensburg, Germany	Drugs	No Action Indicated (NAI)	3005987757
Jul 20, 2012	Ravensburg, Germany	Drugs	No Action Indicated (NAI)	3005987757
Apr 1, 2010	Ravensburg, Germany	Drugs	Voluntary Action Indicated (VAI)	3005987757

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3005987757	Ravensburg, Germany	10	Jul 21, 2023

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) and the FDA: common questions

Has Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) received an FDA warning letter?

No FDA warning letter addressed to the name "Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) received an FDA Form 483?

FDA has not published a Form 483 for "Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)?

The most recent FDA inspection on file ended Jul 21, 2023 at Ravensburg, Germany and was classified VAI. FDA has 10 inspections of Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) on file.

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