Kohjin Life Sciences Co Ltd
FDA import alert and refusal historyTokyo, JapanFEI 3009864303
As of October 26, 2026, Kohjin Life Sciences Co Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 7, 2017, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Antioxidants (food additives for human use) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kohjin Life Sciences Co Ltd
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Antioxidants (food additives for human use)UNAPPROVEDEntry 286-6840845-4Source
Refusal charges, in plain English
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Kohjin Life Sciences Co Ltd
- Is Kohjin Life Sciences Co Ltd on an FDA import alert?
- No listing for Kohjin Life Sciences Co Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from Kohjin Life Sciences Co Ltd?
- Yes. FDA refused 1 shipment line from Kohjin Life Sciences Co Ltd on September 7, 2017. The most recent, on September 7, 2017, was antioxidants (food additives for human use), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Kohjin Life Sciences Co Ltd's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Kohjin Life Sciences Co Ltd's FEI number?
- Kohjin Life Sciences Co Ltd's FDA Establishment Identifier (FEI) is 3009864303.
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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.