PT Marindo Makmur Usahajaya
FDA import alert and refusal historySidoarjo, IndonesiaFEI 3008265582
As of October 26, 2026, PT Marindo Makmur Usahajaya is not on any FDA import alert in SupplierRadar's records; FDA refused 17 of its shipment lines between April 15, 2019 and September 7, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Groupers · NUTRIT LBL
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for PT Marindo Makmur Usahajaya
19 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: GroupersNUTRIT LBLLABELINGEntry AQZ-0620764-4Show 2 linesHide lines
- Refused, GroupersNUTRIT LBLEntry AQZ-0620764-4Source
- Refused, GroupersLABELINGNUTRIT LBLEntry AQZ-0620764-4Source
- Import refusalSource
Refused, 2 lines in one entry: Mahi mahiFILTHYEntry AQZ-0645050-9Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: Mahi mahiFILTHYEntry AQZ-0642616-0Show 2 linesHide lines
2021
2019
- Import refusalSource
Refused, 5 lines in one entry: Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Show 5 linesHide lines
- Refused, Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Source
- Refused, Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Source
- Refused, Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Source
- Refused, Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Source
- Refused, Kingfish (only menticirrhus spp)FILTHYEntry 594-0313762-9Source
- Import refusalSource
Refused, 2 lines in one entry: Snapper (red, gray, malabar, etc.)FILTHYEntry 406-0555842-4Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: Snapper (red, gray, malabar, etc.)FILTHYEntry 594-0302701-0Show 2 linesHide lines
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY15 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about PT Marindo Makmur Usahajaya
- Is PT Marindo Makmur Usahajaya on an FDA import alert?
- No listing for PT Marindo Makmur Usahajaya appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from PT Marindo Makmur Usahajaya?
- Yes. FDA refused 17 shipment lines from PT Marindo Makmur Usahajaya between April 15, 2019 and September 7, 2026. The most recent, on September 7, 2026, was groupers, charged as NUTRIT LBL (nutrition information missing from label).
- Why did FDA refuse PT Marindo Makmur Usahajaya's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 15 lines) and NUTRIT LBL (nutrition information missing from label, 2 lines).
- When was PT Marindo Makmur Usahajaya last inspected by FDA?
- FDA's most recent inspection of PT Marindo Makmur Usahajaya with a final classification is dated February 5, 2019 and was classified NAI (No Action Indicated).
- What is PT Marindo Makmur Usahajaya's FEI number?
- PT Marindo Makmur Usahajaya's FDA Establishment Identifier (FEI) is 3008265582.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.