Khoshnam Fars Co
FDA import alert and refusal historyShiraz, IranFEI 3012198895
As of October 26, 2026, Khoshnam Fars Co is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 22, 2016, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Khoshnam Fars Co
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import refusalRefused, Tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables)NO PROCESSEntry 300-7244850-8Source
Refusal charges, in plain English
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Khoshnam Fars Co
- Is Khoshnam Fars Co on an FDA import alert?
- No listing for Khoshnam Fars Co appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Iran page.
- Has FDA refused shipments from Khoshnam Fars Co?
- Yes. FDA refused 1 shipment line from Khoshnam Fars Co on November 22, 2016. The most recent, on November 22, 2016, was tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Khoshnam Fars Co's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Khoshnam Fars Co's FEI number?
- Khoshnam Fars Co's FDA Establishment Identifier (FEI) is 3012198895.
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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.