Home / Companies / WHITMAN LABORATORIES LTD.

WHITMAN LABORATORIES LTD. FDA Record

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

WHITMAN LABORATORIES LTD. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "WHITMAN LABORATORIES LTD." is on file.

What these totals cover: FDA records filed under the name "WHITMAN LABORATORIES LTD." and its spelling variant "Whitman Laboratories".

Latest inspection: Feb 27, 2026 · 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

WHITMAN LABORATORIES 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	1	0	0	0	0
2025	0	0	0	0	0
2024	0	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	0	0	0	0	0
2018	0	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.

Reviewing WHITMAN LABORATORIES LTD. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check WHITMAN LABORATORIES LTD. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Recent FDA inspections

3 inspections from Aug 5, 2016 to Feb 27, 2026.

Date	Site	Product	Classification	FEI
Feb 27, 2026	Petersfield, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3004347567
May 26, 2021	Petersfield, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3004347567
Aug 5, 2016	Petersfield, United Kingdom	Drugs	Voluntary Action Indicated (VAI)	3004347567

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 3004347567	Petersfield, United Kingdom	3	Feb 27, 2026

WHITMAN LABORATORIES LTD. and the FDA: common questions

Has WHITMAN LABORATORIES LTD. received an FDA warning letter?

No FDA warning letter addressed to the name "WHITMAN LABORATORIES 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 WHITMAN LABORATORIES LTD. received an FDA Form 483?

FDA has not published a Form 483 for "WHITMAN LABORATORIES LTD." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect WHITMAN LABORATORIES LTD.?

The most recent FDA inspection on file ended Feb 27, 2026 at Petersfield, United Kingdom and was classified VAI. FDA has 3 inspections of WHITMAN LABORATORIES LTD. on file.

Need more than this page shows? Ask about WHITMAN LABORATORIES LTD. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.