Actfor,Inc.
FDA import alert and refusal historySasebo, JapanFEI 3011596405
As of October 25, 2026, Actfor,Inc. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between June 23, 2023 and September 5, 2025, most often for artificial coloring not declared (COLOR LBLG).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Ginger root, with sauce · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Actfor,Inc.
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Ginger root, with sauceUNSAFE COLCOLOR LBLGNEEDS FCENO PROCESSEntry 8YW-0004739-8Source
2023
Refusal charges, in plain English
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- 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.
- 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.
- YELLOW #51 refused line
FD&C Yellow No. 5 not declared
The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.
Questions about Actfor,Inc.
- Is Actfor,Inc. on an FDA import alert?
- No listing for Actfor,Inc. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Actfor,Inc.?
- Yes. FDA refused 2 shipment lines from Actfor,Inc. between June 23, 2023 and September 5, 2025. The most recent, on September 5, 2025, was ginger root, with sauce, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Actfor,Inc.'s shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and NEEDS FCE (processor not registered for canned or acidified foods, 1 line).
- What is Actfor,Inc.'s FEI number?
- Actfor,Inc.'s FDA Establishment Identifier (FEI) is 3011596405.
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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.