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Lofthouse Of Fleetwood Ltd. FDA Record

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

Latest inspection VAI · Mar 22, 2023
No warning letters matched by name

Inspections 3

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Lofthouse Of Fleetwood Ltd. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Lofthouse Of Fleetwood Ltd." is on file.

What these totals cover: FDA records filed under the name "Lofthouse Of Fleetwood Ltd." and its spelling variant "Lofthouse Of Fleetwood".

Latest inspection: Mar 22, 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	3	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

Lofthouse Of Fleetwood Ltd.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Lofthouse Of Fleetwood Ltd.: 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	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	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.

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Recent FDA inspections

3 inspections from Dec 5, 2014 to Mar 22, 2023.

Date	Site	Product	Classification	FEI
Mar 22, 2023	Fleetwood, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3000291907
Aug 24, 2018	Fleetwood, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3000291907
Dec 5, 2014	Fleetwood, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3000291907

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 3000291907	Fleetwood, United Kingdom	3	Mar 22, 2023

Lofthouse Of Fleetwood Ltd. and the FDA: common questions

Has Lofthouse Of Fleetwood Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Lofthouse Of Fleetwood Ltd." 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 Lofthouse Of Fleetwood Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Lofthouse Of Fleetwood Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Lofthouse Of Fleetwood Ltd.?

The most recent FDA inspection on file ended Mar 22, 2023 at Fleetwood, United Kingdom and was classified VAI. FDA has 3 inspections of Lofthouse Of Fleetwood Ltd. on file.

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