Home / Companies / Unilever Philippines, Inc. - Cavite Factory

Unilever Philippines, Inc. - Cavite Factory FDA Record

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

Latest inspection VAI · Dec 13, 2023
No warning letters matched by name

Inspections 4

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Unilever Philippines, Inc. - Cavite Factory has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Unilever Philippines, Inc. - Cavite Factory" is on file.

What these totals cover: FDA records filed under the name "Unilever Philippines, Inc. - Cavite Factory".

Latest inspection: Dec 13, 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	4	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

Unilever Philippines, Inc. - Cavite Factory's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Unilever Philippines, Inc. - Cavite Factory: 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	2	0	0	0	0
2022	0	0	0	0	0
2021	0	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.

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Recent FDA inspections

4 inspections from May 10, 2017 to Dec 13, 2023.

Date	Site	Product	Classification	FEI
Dec 13, 2023	Gen. Trias, Philippines	Drugs	Voluntary Action Indicated (VAI)	2000001160
Aug 16, 2023	Gen. Trias, Philippines	Food/Cosmetics	No Action Indicated (NAI)	2000001160
Feb 8, 2019	Gen. Trias, Philippines	Food/Cosmetics	Voluntary Action Indicated (VAI)	2000001160
May 10, 2017	Gen. Trias, Philippines	Drugs	Voluntary Action Indicated (VAI)	2000001160

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 2000001160	Gen. Trias, Philippines	4	Dec 13, 2023

Unilever Philippines, Inc. - Cavite Factory and the FDA: common questions

Has Unilever Philippines, Inc. - Cavite Factory received an FDA warning letter?

No FDA warning letter addressed to the name "Unilever Philippines, Inc. - Cavite Factory" 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 Unilever Philippines, Inc. - Cavite Factory received an FDA Form 483?

FDA has not published a Form 483 for "Unilever Philippines, Inc. - Cavite Factory" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Unilever Philippines, Inc. - Cavite Factory?

The most recent FDA inspection on file ended Dec 13, 2023 at Gen. Trias, Philippines and was classified VAI. FDA has 4 inspections of Unilever Philippines, Inc. - Cavite Factory on file.

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