PT. ARTA MINA TAMA FDA Record

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

  • Latest inspection VAI · May 27, 2011
  • No warning letters matched by name
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

PT. ARTA MINA TAMA has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "PT. ARTA MINA TAMA" is on file.

What these totals cover: FDA records filed under the name "PT. ARTA MINA TAMA".

Latest inspection
May 27, 2011 · 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 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on May 27, 2011.

DateSiteProductClassificationFEI
May 27, 2011Jakarta, IndonesiaFood/CosmeticsVoluntary Action Indicated (VAI)3010141089
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 3010141089Jakarta, Indonesia1May 27, 2011

PT. ARTA MINA TAMA and the FDA: common questions

Has PT. ARTA MINA TAMA received an FDA warning letter?

No FDA warning letter addressed to the name "PT. ARTA MINA TAMA" 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 PT. ARTA MINA TAMA received an FDA Form 483?

FDA has not published a Form 483 for "PT. ARTA MINA TAMA" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect PT. ARTA MINA TAMA?

The most recent FDA inspection on file ended May 27, 2011 at Jakarta, Indonesia and was classified VAI. FDA has 1 inspection of PT. ARTA MINA TAMA on file.

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