Mommy Gina Tuna Resources (MGTR), Inc FDA Record

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

  • Latest inspection VAI · May 14, 2009
  • Last warning letter 2013
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 1 Latest Dec 4, 2013
510(k) clearances 0 None on file

Mommy Gina Tuna Resources (MGTR), Inc has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Mommy Gina Tuna Resources (MGTR), Inc, the most recent on Dec 4, 2013.

What these totals cover: FDA records filed under the name "Mommy Gina Tuna Resources (MGTR), Inc" and its spelling variant "Mommy Gina Tuna Resources (Mgtr)".

Latest inspection
May 14, 2009 · 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
Inspections1Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Reviewing Mommy Gina Tuna Resources (MGTR), Inc 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 Mommy Gina Tuna Resources (MGTR), Inc 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

Mommy Gina Tuna Resources (MGTR), Inc FDA Warning Letters

1 warning letter on Dec 4, 2013.

IssuedSubjectIssuing officeClose-out letter
Dec 4, 2013 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

1 inspection on May 14, 2009.

DateSiteProductClassificationFEI
May 14, 2009General Santos City, PhilippinesFood/CosmeticsVoluntary Action Indicated (VAI)3004282036
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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Mommy Gina Tuna Resources (MGTR), Inc: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Dec 4, 2013.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3004282036General Santos City, Philippines1May 14, 2009

Mommy Gina Tuna Resources (MGTR), Inc and the FDA: common questions

Has Mommy Gina Tuna Resources (MGTR), Inc received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Mommy Gina Tuna Resources (MGTR), Inc. The most recent is dated Dec 4, 2013.

Has Mommy Gina Tuna Resources (MGTR), Inc received an FDA Form 483?

FDA has not published a Form 483 for "Mommy Gina Tuna Resources (MGTR), Inc" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Mommy Gina Tuna Resources (MGTR), Inc?

The most recent FDA inspection on file ended May 14, 2009 at General Santos City, Philippines and was classified VAI. FDA has 1 inspection of Mommy Gina Tuna Resources (MGTR), Inc on file.

Need more than this page shows? Ask about Mommy Gina Tuna Resources (MGTR), Inc 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.