Appare Suisan Himeji Branch
FDA import alert and refusal historyHimeji, JapanFEI 3010233781
Recorded by FDA as APPARE SUISAN HIMEJI BRANCH
As of October 26, 2026, Appare Suisan Himeji Branch is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between July 12, 2017 and September 19, 2017, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Anchovy · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Appare Suisan Himeji Branch
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- MFR INSAN2 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about Appare Suisan Himeji Branch
- Is Appare Suisan Himeji Branch on an FDA import alert?
- No listing for Appare Suisan Himeji Branch 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 Appare Suisan Himeji Branch?
- Yes. FDA refused 4 shipment lines from Appare Suisan Himeji Branch between July 12, 2017 and September 19, 2017. The most recent, on September 19, 2017, was anchovy, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Appare Suisan Himeji Branch's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 2 lines).
- What is Appare Suisan Himeji Branch's FEI number?
- Appare Suisan Himeji Branch's FDA Establishment Identifier (FEI) is 3010233781.
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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.