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KVP Pharma Veterin Produkte GmbH FDA Record

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

KVP Pharma Veterin Produkte GmbH has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "KVP Pharma Veterin Produkte GmbH" is on file.

What these totals cover: FDA records filed under the name "KVP Pharma Veterin Produkte GmbH" and its spelling variant "Kvp Pharma Veterin Produkte".

Latest inspection: Mar 24, 2023 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	4	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

KVP Pharma Veterin Produkte GmbH's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

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	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	0	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

4 inspections from Jun 17, 2011 to Mar 24, 2023.

Date	Site	Product	Classification	FEI
Mar 24, 2023	Kiel, Germany	Veterinary	Voluntary Action Indicated (VAI)	3004159824
Apr 28, 2017	Kiel, Germany	Veterinary	No Action Indicated (NAI)	3004159824
Apr 30, 2015	Kiel, Germany	Veterinary	No Action Indicated (NAI)	3004159824
Jun 17, 2011	Kiel, Germany	Veterinary	Voluntary Action Indicated (VAI)	3004159824

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 3004159824	Kiel, Germany	4	Mar 24, 2023

KVP Pharma Veterin Produkte GmbH and the FDA: common questions

Has KVP Pharma Veterin Produkte GmbH received an FDA warning letter?

No FDA warning letter addressed to the name "KVP Pharma Veterin Produkte GmbH" 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 KVP Pharma Veterin Produkte GmbH received an FDA Form 483?

FDA has not published a Form 483 for "KVP Pharma Veterin Produkte GmbH" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect KVP Pharma Veterin Produkte GmbH?

The most recent FDA inspection on file ended Mar 24, 2023 at Kiel, Germany and was classified VAI. FDA has 4 inspections of KVP Pharma Veterin Produkte GmbH on file.

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