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Haupt Pharma Wolfratshausen GmbH FDA Record

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

Latest inspection VAI · Nov 15, 2022
No warning letters matched by name

Inspections 6

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Haupt Pharma Wolfratshausen GmbH has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Haupt Pharma Wolfratshausen GmbH" is on file.

What these totals cover: FDA records filed under the name "Haupt Pharma Wolfratshausen GmbH" and its spelling variant "Haupt Pharma Wolfratshausen".

Latest inspection: Nov 15, 2022 · 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	6	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

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

Haupt Pharma Wolfratshausen GmbH: 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	0	0	0	0	0
2022	1	0	0	0	0
2021	0	0	0	0	0
2020	1	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

6 inspections from May 11, 2012 to Nov 15, 2022.

Date	Site	Product	Classification	FEI
Nov 15, 2022	Wolfratshausen, Germany	Drugs	Voluntary Action Indicated (VAI)	3000310230
Aug 5, 2020	Wolfratshausen, Germany	Drugs	Voluntary Action Indicated (VAI)	3000310230
Oct 20, 2017	Wolfratshausen, Germany	Veterinary	Voluntary Action Indicated (VAI)	3000310230
Apr 9, 2016	Wolfratshausen, Germany	Drugs	Voluntary Action Indicated (VAI)	3000310230
Mar 18, 2014	Wolfratshausen, Germany	Veterinary	Voluntary Action Indicated (VAI)	3000310230
May 11, 2012	Wolfratshausen, Germany	Drugs	Voluntary Action Indicated (VAI)	3000310230

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 3000310230	Wolfratshausen, Germany	6	Nov 15, 2022

Haupt Pharma Wolfratshausen GmbH and the FDA: common questions

Has Haupt Pharma Wolfratshausen GmbH received an FDA warning letter?

No FDA warning letter addressed to the name "Haupt Pharma Wolfratshausen 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 Haupt Pharma Wolfratshausen GmbH received an FDA Form 483?

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

When did the FDA last inspect Haupt Pharma Wolfratshausen GmbH?

The most recent FDA inspection on file ended Nov 15, 2022 at Wolfratshausen, Germany and was classified VAI. FDA has 6 inspections of Haupt Pharma Wolfratshausen GmbH on file.

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