Four points of control
We split the risk into four questions: whose product, how it was frozen, what was tested,
and how it is labelled.
1 · Supplier qualification
Before a plant enters our supplier list it must produce export registration, a
third-party audit report, recent microbiological and residue testing, and a customer
reference we can actually call. A plant that fails review does not get bought from,
whatever the price.
Depending on species, we require suppliers to hold one or more of:
HACCPBAPASC
MSCBRCGSISO 22000
2 · Cold chain control
After blast freezing at origin, product is held at −18°C or below end to end. Reefers are
pre-cooled and set-point logged before loading, data loggers travel with the cargo, and
containers move from port straight into third-party cold storage.
- Pre-cool and set-point record before loading
- In-transit data logger, available on delivery
- Cold storage temperature logs retained by lot
- Refrigerated final-mile delivery; insulated totes on short runs
3 · Testing & acceptance
The plant supplies lot-level test results before shipment. On arrival we sample against a
written plan — appearance, odour, deglazed net weight, core temperature and pack
integrity — and send to an independent laboratory when anything looks off.
Typical scope: pathogens, antibiotic residues where the species warrants, histamine on
scombroid species, heavy metals, and harvest-area biotoxin records for bivalves.
4 · Labelling & filing
Labels are reviewed against US requirements: market and scientific name, country of
origin, farmed or wild, net weight statement, allergens, establishment number, storage
conditions and thaw instructions. SIMP supply-chain data is filed for listed species and
FDA Prior Notice is submitted before arrival.