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Wanbury Ltd.

FDA Regulatory Profile

Wanbury Ltd. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Wanbury Ltd." and its spelling variants "Wanbury", "Wanbury Limited".

Latest inspection: Jun 14, 2024 · NAI

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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	8	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

Wanbury Ltd.'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	0	0	0	0	0
2020	0	0	0	0	0
2019	0	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

8 inspections from Feb 18, 2009 to Jun 14, 2024.

Date	Site	Product	Classification	FEI
Jun 14, 2024	Patalganga, India	Drugs	No Action Indicated (NAI)	3003227148
Mar 2, 2018	Tanuku, India	Drugs	Voluntary Action Indicated (VAI)	3002980818
Sep 29, 2016	Patalganga, India	Drugs	Voluntary Action Indicated (VAI)	3003227148
Jul 1, 2016	Tanuku, India	Drugs	Voluntary Action Indicated (VAI)	3002980818
May 9, 2013	Patalganga, India	Drugs	No Action Indicated (NAI)	3003227148
Aug 3, 2012	Tanuku, India	Drugs	No Action Indicated (NAI)	3002980818
Oct 30, 2009	Patalganga, India	Drugs	Voluntary Action Indicated (VAI)	3003227148
Feb 18, 2009	Tanuku, India	Drugs	Voluntary Action Indicated (VAI)	3002980818

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

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3003227148	Patalganga, India	4	Jun 14, 2024
FEI 3002980818	Tanuku, India	4	Mar 2, 2018

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