Liwayway Marketing Corporation FDA Record

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

Liwayway Marketing Corporation has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Liwayway Marketing Corporation" is on file.

What these totals cover: FDA records filed under the name "Liwayway Marketing Corporation".

Latest inspection
Jul 26, 2023 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Liwayway Marketing Corporation's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Liwayway Marketing Corporation: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202000000
201900000
201800000
201710000

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 Liwayway Marketing Corporation 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 Liwayway Marketing Corporation 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

2 inspections from Oct 24, 2017 to Jul 26, 2023.

DateSiteProductClassificationFEI
Jul 26, 2023Imus, PhilippinesFood/CosmeticsVoluntary Action Indicated (VAI)3006313016
Oct 24, 2017Imus, PhilippinesFood/CosmeticsVoluntary Action Indicated (VAI)3006313016
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.

FacilityLocationInspectionsLatest
FEI 3006313016Imus, Philippines2Jul 26, 2023

Liwayway Marketing Corporation and the FDA: common questions

Has Liwayway Marketing Corporation received an FDA warning letter?

No FDA warning letter addressed to the name "Liwayway Marketing Corporation" 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 Liwayway Marketing Corporation received an FDA Form 483?

FDA has not published a Form 483 for "Liwayway Marketing Corporation" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Liwayway Marketing Corporation?

The most recent FDA inspection on file ended Jul 26, 2023 at Imus, Philippines and was classified VAI. FDA has 2 inspections of Liwayway Marketing Corporation on file.

Need more than this page shows? Ask about Liwayway Marketing Corporation 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.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.