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Ferring GmbH

FDA Regulatory Profile

Ferring GmbH has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

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

Latest inspection: Feb 29, 2024 · 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	7	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

Ferring 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	1	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	1	0	0	0	0
2020	0	0	0	0	0
2019	1	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.

Recent FDA inspections

7 inspections from Nov 19, 2010 to Feb 29, 2024.

Date	Site	Product	Classification	FEI
Feb 29, 2024	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Sep 30, 2021	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Aug 23, 2019	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Jan 27, 2017	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Nov 11, 2014	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Oct 26, 2012	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979
Nov 19, 2010	Kiel, Germany	Drugs	Voluntary Action Indicated (VAI)	3002806979

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 3002806979	Kiel, Germany	7	Feb 29, 2024

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