Orihiro Co. Ltd
FDA import alert and refusal historyTakasaki, JapanFEI 3015829751
Recorded by FDA as ORIHIRO CO. LTD
As of October 26, 2026, Orihiro Co. Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 4, 2023, most often for foreign ob (FOREIGN OB).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Gel cups, fruit flavored · FOREIGN OB
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Orihiro Co. Ltd
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Gel cups, fruit flavoredFOREIGN OBNO ENGLISHEntry 799-5674847-9Source
Refusal charges, in plain English
- FOREIGN OB1 refused line
FOREIGN OB
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Orihiro Co. Ltd
- Is Orihiro Co. Ltd on an FDA import alert?
- No listing for Orihiro 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 Orihiro Co. Ltd?
- Yes. FDA refused 1 shipment line from Orihiro Co. Ltd on October 4, 2023. The most recent, on October 4, 2023, was gel cups, fruit flavored, charged as FOREIGN OB (foreign ob).
- Why did FDA refuse Orihiro Co. Ltd's shipments?
- The most frequent charges are FOREIGN OB (foreign ob, 1 line) and NO ENGLISH (required label information not in english, 1 line).
- What is Orihiro Co. Ltd's FEI number?
- Orihiro Co. Ltd's FDA Establishment Identifier (FEI) is 3015829751.
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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.