PT. Agri Spice Indonesia
FDA import alert and refusal historyKota Bandar, IndonesiaFEI 3004396847
As of October 26, 2026, PT. Agri Spice Indonesia is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 27, 2024, 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
- Nutmeg, ground, cracked (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT. Agri Spice Indonesia
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
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.
Questions about PT. Agri Spice Indonesia
- Is PT. Agri Spice Indonesia on an FDA import alert?
- No listing for PT. Agri Spice Indonesia 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. Agri Spice Indonesia?
- Yes. FDA refused 1 shipment line from PT. Agri Spice Indonesia on September 27, 2024. The most recent, on September 27, 2024, was nutmeg, ground, cracked (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse PT. Agri Spice Indonesia's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was PT. Agri Spice Indonesia last inspected by FDA?
- FDA's most recent inspection of PT. Agri Spice Indonesia with a final classification is dated October 9, 2018 and was classified VAI (Voluntary Action Indicated).
- What is PT. Agri Spice Indonesia's FEI number?
- PT. Agri Spice Indonesia's FDA Establishment Identifier (FEI) is 3004396847.
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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.