Pt. Mikie Oleo Nabati Industri
FDA import alert and refusal historyBekasi, IndonesiaFEI 3009554208
As of October 26, 2026, Pt. Mikie Oleo Nabati Industri (Bekasi, Indonesia) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for bulk shortening, published by FDA on January 8, 2016, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Pt. Mikie Oleo Nabati Industri
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 99-39red listBulk ShorteningSource
2015
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and EconSource
Questions about Pt. Mikie Oleo Nabati Industri
- Is Pt. Mikie Oleo Nabati Industri on an FDA import alert?
- Yes. As of October 26, 2026, Pt. Mikie Oleo Nabati Industri is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for bulk shortening; FDA published the listing on January 8, 2016.
- Has FDA refused shipments from Pt. Mikie Oleo Nabati Industri?
- No FDA import refusals for Pt. Mikie Oleo Nabati Industri appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Pt. Mikie Oleo Nabati Industri last inspected by FDA?
- FDA's most recent inspection of Pt. Mikie Oleo Nabati Industri with a final classification is dated August 19, 2015 and was classified OAI (Official Action Indicated).
- What is Pt. Mikie Oleo Nabati Industri's FEI number?
- Pt. Mikie Oleo Nabati Industri's FDA Establishment Identifier (FEI) is 3009554208.
- Can shipments from Pt. Mikie Oleo Nabati Industri still enter the U.S.?
- Shipments of bulk shortening from Pt. Mikie Oleo Nabati Industri can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.