Quote within 24 hours Free DFM review ISO 9001 & ISO 13485 certified NDA signed before drawing review
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Quality & documentation

Inspection is a sequence, not a promise

Everything below happens on every order unless your drawing says otherwise. If a step cannot be met, you hear it before the batch starts — not after.

ISO 9001:2015ISO 13485:2016CMM report included
Certification

What we are certified for — and what we are not

We list only certificates that exist and can be verified with the issuing body. If your programme requires a standard we do not hold, we will say so on the first call rather than on the PO.

ISO

ISO 9001:2015

Quality management system covering quoting, production planning, inspection and corrective action.

Certified since 2016 · scope: machining & assembly
13485

ISO 13485:2016

Medical device quality management. Enables instrument housings and components with full device-file traceability.

Certified since 2019 · scope: precision components
LAB

In-house calibration

CMM and gauges calibrated on a 12-month cycle against traceable standards; certificates kept with the batch record.

12-month cycle · records on file
Inspection sequence

Five gates between the raw bar and the carton

  1. Incoming material

    Heat number checked against the mill certificate, then verified with the spectrometer on stainless and aluminium. Non-conforming bar is quarantined before it reaches a machine.

  2. First article inspection

    Full drawing layout on the first part of a new programme, including features not called out as critical. The batch does not start until the FAI is signed.

  3. In-process control

    Operators check designated features every two hours; QC audits the records twice a shift. Renishaw probes verify datum and bore position on the machine.

  4. Final inspection

    CMM programme written from your drawing, not from our model. Report lists every dimension with measured value and deviation.

  5. Packaging & dispatch

    Wrap, EPE, foam, carton or case. Photographed before sealing; the photo set travels with the shipment documents.

Documents are issued as PDF with the batch number. If your QA system needs a specific template, send it and we will fill yours in instead.

Metrology

The measuring room is bigger than the sales office

Inspection capacity is what decides whether a 0.008 mm flatness call-out is real or aspirational.

Swipe sideways for more columns →
EquipmentQtyBrand / typeCapability
Coordinate measuring machines4Zeiss Contura, Hexagon Global S0.9 + L/350 µm
Optical comparators / VMM3Mitutoyo QV±1.5 µm
Surface roughness testers5Mitutoyo SJ-210Ra 0.05–10 µm
Hardness testers3Rockwell / VickersHRC, HV
Spectrometers2Optical emissionMaterial verification
X-ray / CT (partner)1On requestInternal features
Swipe sideways for more columns →
DocumentWhat it containsDefault
Material certificateEN 10204 3.1 mill cert with heat number, chemical composition and mechanical properties.Included
Dimensional inspection reportEvery dimension on your drawing, measured value against nominal and tolerance band.Included
First article inspection (FAI)AS9102-style layout for new parts, signed before the batch is released.Included
Certificate of conformanceSigned statement that the parts meet the drawing and the PO.Included
CMM reportRaw coordinate output plus the plotted tolerance bands for critical features.Included
PPAP packageLevels 1–5 on request, with control plan, MSA and capability studies.Included
Surface / finish reportCoating thickness, salt-spray hours and colour match where specified.Included
RoHS / REACH declarationMaterial declarations for electronic and consumer programmes.Included
Quality engineer reviewing parts with a customer during a plant audit
When something goes wrong

Non-conformance is handled in writing, within 48 hours

Every complaint gets a numbered NC report: what was found, which batch, root cause, containment, corrective action and the date it was verified. You get the same document we use internally.

If the fault is ours, we remake or refund — and the report goes out even when the value is small, because that is the record your own auditor will ask for.

  • 48 h initial response with containment
  • 5 years batch records retained
  • 100% remake or refund on our defects
  • Annual internal audit + management review

Need the quality pack before you commit?

Ask for a redacted sample of any document above — FAI, CMM report, PPAP or material cert.