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Thymoorgan Pharmazie Gmbh

FDA Regulatory Profile

Thymoorgan Pharmazie Gmbh has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Thymoorgan Pharmazie Gmbh" and its spelling variant "Thymoorgan Pharmazie".

Latest inspection: Mar 26, 2025 · VAI

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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	9	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Thymoorgan Pharmazie 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	1	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	1	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	1	0	0	0	0
2017	0	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.

Recent FDA inspections

9 inspections from Feb 9, 2010 to Mar 26, 2025.

Date	Site	Product	Classification	FEI
Mar 26, 2025	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821
Apr 25, 2023	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821
Oct 6, 2022	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821
Jun 20, 2019	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821
Apr 23, 2018	Goslar, Germany	Drugs	No Action Indicated (NAI)	3002320821
Dec 16, 2016	Goslar, Germany	Drugs	No Action Indicated (NAI)	3002320821
Sep 24, 2015	Goslar, Germany	Drugs	No Action Indicated (NAI)	3002320821
May 22, 2014	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821
Feb 9, 2010	Goslar, Germany	Drugs	Voluntary Action Indicated (VAI)	3002320821

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 3002320821	Goslar, Germany	9	Mar 26, 2025

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