Yamahide Shokuhin, Inc.
FDA import alert and refusal historyMiki, JapanFEI 3004249056
As of October 26, 2026, Yamahide Shokuhin, Inc. (Miki, Japan) is on the red list of FDA Import Alert 16-74 (Uneviscerated salt-cured, dried, smoked or fermented fish) for anchovy, published by FDA on July 12, 2011, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-74 · red list
- Last import refusal
- Anchovy · MFR INSAN
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Yamahide Shokuhin, Inc.
4 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2018
2014
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 16-74red listAnchovySource
Refusal charges, in plain English
- MFR INSAN1 refused line
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 Yamahide Shokuhin, Inc.
- Is Yamahide Shokuhin, Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Yamahide Shokuhin, Inc. is on the red list of FDA Import Alert 16-74, “Uneviscerated salt-cured, dried, smoked or fermented fish”, for anchovy; FDA published the listing on July 12, 2011.
- Has FDA refused shipments from Yamahide Shokuhin, Inc.?
- Yes. FDA refused 1 shipment line from Yamahide Shokuhin, Inc. on April 17, 2018. The most recent, on April 17, 2018, was anchovy, charged as MFR INSAN (insanitary manufacturing, processing or packing).
- Why did FDA refuse Yamahide Shokuhin, Inc.'s shipments?
- The most frequent charge is MFR INSAN (insanitary manufacturing, processing or packing, 1 line).
- When was Yamahide Shokuhin, Inc. last inspected by FDA?
- FDA's most recent inspection of Yamahide Shokuhin, Inc. with a final classification is dated July 5, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Yamahide Shokuhin, Inc.'s FEI number?
- Yamahide Shokuhin, Inc.'s FDA Establishment Identifier (FEI) is 3004249056.
- Can shipments from Yamahide Shokuhin, Inc. still enter the U.S.?
- Shipments of anchovy from Yamahide Shokuhin, Inc. can be detained without physical examination under Import Alert 16-74; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
Buying from Yamahide Shokuhin, Inc.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.