Farshid Foodstuff Industry L.L.C
FDA import alert and refusal historyDubai, United Arab EmiratesFEI 3014478536
As of October 26, 2026, Farshid Foodstuff Industry L.L.C is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 1, 2024, most often for color additive unsafe under section 721 (UNSAFE COL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Henna · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Farshid Foodstuff Industry L.L.C
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, HennaUNSAFE COLEntry 772-0284693-5Source
Refusal charges, in plain English
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Farshid Foodstuff Industry L.L.C
- Is Farshid Foodstuff Industry L.L.C on an FDA import alert?
- No listing for Farshid Foodstuff Industry L.L.C appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Arab Emirates page.
- Has FDA refused shipments from Farshid Foodstuff Industry L.L.C?
- Yes. FDA refused 1 shipment line from Farshid Foodstuff Industry L.L.C on November 1, 2024. The most recent, on November 1, 2024, was henna, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Farshid Foodstuff Industry L.L.C's shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Farshid Foodstuff Industry L.L.C's FEI number?
- Farshid Foodstuff Industry L.L.C's FDA Establishment Identifier (FEI) is 3014478536.
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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.