ISO
9001:2015 Certified
Every part Great light ships has been inspected, documented, and released against a verifiable standard. Not a supplier claim. A documented, auditable commitment.
12+ years of CNC machining quality engineering · Primary DFM & inspection protocol reviewer · Oversees quality gate decisions on all aerospace, medical, and automotive programs · Reviewed 1,200+ part drawings annually
When a B2B buyer asks “how do we know your parts meet spec?” — the honest answer is not “because we say so.” It is: here is the CNC machining inspection data, here is the CMM report, here is the material certification, and here is the documented quality system that produced all of it. At Great Light, quality is not a department — it is the engineering framework through which every production decision is made, from the moment your drawing arrives to the moment your parts leave our loading dock.
This page explains exactly what our quality assurance system consists of, how it operates, what documentation it generates, and why it meets the requirements of aerospace, automotive, and medical supply chains simultaneously — under three independently audited certifications.
Most CNC suppliers hold one certification. Great Light holds three — simultaneously, all current, all third-party audited. This is not a coincidence; it is a deliberate investment in the quality infrastructure required to serve regulated supply chains in aerospace, automotive, and medical simultaneously.
The foundation standard. Covers every process that affects product quality — from order review and DFM through manufacturing, inspection, and delivery. Requires documented control plans, calibration management, internal audit, and management review.
The mandatory quality standard for Tier 1 and Tier 2 automotive suppliers. Includes FMEA, SPC process capability monitoring, PPAP documentation (Levels 1–3), control plans, and Measurement System Analysis (MSA / Gauge R&R).
The quality standard for medical device manufacturing. Covers design control, risk management, batch traceability, material verification, and the documentation required for regulatory submissions (FDA, CE). Applies to all Great Light medical component programs.
A supplier who relies on final inspection to find non-conforming parts is not controlling quality — they are sorting defects after the cost has already been incurred. Every scrapped part represents 100% of its machining time and material cost consumed with zero value delivered. Great Light’s quality approach is prevention-first.
🔍 Sourcing parts for a regulated application? Upload your drawing — Great Light’s engineering team reviews quality requirements alongside manufacturability and returns a quote with full quality documentation options within 4–8 hours. Request a quality-first quote →
What separates a quality-controlled shop from one that merely has a CMM? The answer is when inspection happens. Catching a non-conformance after the part is fully machined means all the machining time is already spent. Great Light’s 5-stage protocol inserts measurement checkpoints at each critical transition during machining — turning inspection from a final verdict into a continuous dialogue with the process.
Post-processing introduces dimensional change: Type II anodize adds 5–12µm outward per surface; Type III hard anodize adds 12–37µm; electroless nickel adds 5–25µm; heat treatment distorts geometry. All of these effects are predicted and pre-compensated in the machining program — but must be verified after the fact.

The credibility of any tolerance claim rests entirely on the measurement equipment available to verify it. Great Light maintains a fully equipped in-house metrology lab — not outsourced, not a shared facility — with all instruments calibrated on defined schedules and traceable to national standards.
| Instrument | Resolution | Application | Calibration Interval |
|---|---|---|---|
| CMM (Coordinate Measuring Machine) | ±0.001mm uncertainty | 3D geometry, GD&T all characteristics, automated production programs | 6 months |
| Digital Outside Micrometer | 0.001mm | OD diameters, shaft sizes, wall thicknesses | 12 months |
| Digital Bore Gauge / Air Gauge | 0.001mm | Internal diameters, bearing bores, reamed holes | 12 months |
| Surface Profilometer (Ra/Rz) | 0.01µm | Surface roughness measurement: Ra, Rz, Rq on functional surfaces | 12 months |
| XRF Analyzer (X-ray Fluorescence) | Elemental % | Positive Material Identification (PMI) — Ti, Inconel, SS alloy verification | Annual |
| Optical Comparator / Vision System | 0.001mm | Thread profiles, small features, contour verification | 12 months |
| Hardness Tester (Rockwell / Vickers) | ±0.5 HRC | Post-heat-treat hardness verification, surface treatment batch release | 6 months |
| Thread Gauges (Go/No-Go) | Class 6H/6g | Thread fit and tolerance class verification for all thread forms | On wear check |
A First Article Inspection tells you one part met tolerance. What tells you the thousandth part will also meet tolerance? Statistical Process Control (SPC) does. By measuring and plotting key dimensions at defined intervals during production, Great Light detects process drift before it produces out-of-tolerance parts — not after. The control chart is a real-time early-warning system, not a historical archive.
| Cpk Value | Sigma Level | Defect Rate (ppm) | Great Light Assessment |
|---|---|---|---|
| < 1.00 | < 3σ | > 2,700 ppm | ❌ Not capable — not acceptable for production |
| 1.00–1.33 | 3–4σ | 64–2,700 ppm | ⚠️ Marginal — requires 100% inspection + improvement plan |
| ≥ 1.33 | 4σ | 64 ppm | ✅ Great Light minimum production standard |
| ≥ 1.67 | 5σ | 0.6 ppm | ⭐ Preferred for safety-critical & medical applications |
| ≥ 2.00 | 6σ | < 0.002 ppm | ⭐⭐ Six Sigma — targeted for life-critical applications |
The First Article Inspection is the formal, documented verification that the first production part meets every requirement on the engineering drawing — before series production continues. For aerospace programs, Great Light structures FAI per AS9102B methodology. For automotive programs, PPAP documentation (Levels 1–3) is available under IATF 16949. Both are supported; specify your requirement at RFQ stage.

| FAI Element | Description | Standard Reference |
|---|---|---|
| Ballooned Drawing | Every characteristic individually numbered; serves as reference index for all measurements | AS9102 / AIAG PPAP |
| Actual Measured Values | Nominal, tolerance, and actual value for every ballooned dimension — no omissions | AS9102 Form 1 |
| Pass/Fail Disposition | Clear conformance status per characteristic; overall lot disposition | AS9102 / ISO 10012 |
| Measurement Method | Instrument type documented for each characteristic — enables audit of measurement system | AS9102 / MSA |
| Material Certificate Reference | MTR heat number cross-referenced to FAI part for full material traceability | AS9102 / ISO 13485 |
| Special Process Records | Heat treat certificate, anodize/plating certificate, NDT report where applicable | AS9102 / NADCAP |
| Surface Finish Data | Ra profilometer measurements on all functional surface finish callouts | ISO 4287 / ASME B46.1 |
A part machined to perfect tolerances from the wrong material is a non-conforming part. Material verification is not optional — it is the first gate in Great Light’s quality system, and it applies before a single tool engages the workpiece.
No quality system is perfect. What separates a mature quality system from an immature one is how it responds to quality events. Great Light’s Non-Conformance Report (NCR) and Corrective and Preventive Action (CAPA) process ensures every quality event — however small — is documented, root-caused, and permanently corrected. And if a non-conformance affects your order, you hear about it before the parts ship — not after.
Non-conformance identified at any stage → immediate red-tag quarantine. No non-conforming part advances in the process or reaches shipping.
For any non-conformance affecting your order, We notifies the customer within 24 hours — before disposition decision. Customer approval required for any non-conforming shipment.
5-Why or Fishbone root cause analysis. Corrective action defined, assigned, implemented, and verified on the next production run of the same part number.
Great Light’s quality documentation transforms a shipment of machined parts into a fully auditable, traceable supply chain record. Every document is issued against a specific lot, references the purchase order and drawing revision, and is retained per the schedule below. Which documents does your program require? Specify at RFQ stage — we will confirm availability and include them in your shipment.

| Document | Included Standard? | Key Content | Applicable To |
|---|---|---|---|
| Certificate of Conformance (COC) | ✅ All Orders | Declares parts conform to drawing, specification, and PO. Includes lot number, revision, supplier info. | All B2B orders — standard |
| Material Test Report (MTR) | ✅ All Metal | Mill-certified chemical composition + mechanical properties. Heat number traceable to raw material mill. | Aerospace, medical, structural |
| First Article Inspection (FAI) | On Request | Ballooned drawing + all feature actual values + pass/fail + measurement method. AS9102B compatible. | Aerospace AS9100, Medical, Automotive |
| CMM Dimensional Report | On Request | Batch sampling or 100% critical dimension actual values. AQL level. CMM data with measurement uncertainty. | Precision production orders |
| Surface Finish Certificate | On Request | Ra/Rz actual values + profilometer scan data compared to drawing requirement. | Sealing surfaces, bearing surfaces, medical devices |
| Heat Treatment Certificate | When Applicable | Time-temperature curve, hardness test results HRC/HV, batch traceability. | Hardened steel, aerospace fasteners |
| Plating / Anodize Certificate | When Applicable | Process specification, coating thickness measurements, bath certification records. | Anodized, plated, electroless nickel parts |
| PPAP Documentation | On Request | PSW, dimensional results, Cpk data, control plan, PFMEA. Levels 1–3 per AIAG PPAP 4th Edition. | Automotive Tier 1/2 production programs |

Great Light holds three simultaneous ISO certifications: ISO 9001:2015 (general quality management system covering all manufacturing operations), IATF 16949:2016 (automotive supply chain quality — mandatory for Tier 1/2 automotive suppliers), and ISO 13485:2016 (medical device manufacturing quality). All three are current and maintained through annual independent third-party audits. Certificate copies are available on request.
Our uses in-house Coordinate Measuring Machine (CMM) equipment with ±0.001mm measurement uncertainty per ISO 14253-1 to verify all critical dimensions. For production runs, automated CMM programs written during First Article Inspection are re-run on every subsequent inspection lot, ensuring measurement repeatability and eliminating operator-to-operator variation. 100% of critical features are CMM-verified on precision orders before shipment. The CMM operates in a temperature-controlled room at 20°C ±1°C per ISO 1 international reference conditions.
Every Great Light order includes a Certificate of Conformance (COC) as standard. All metal orders include Material Test Reports (MTR). On request: First Article Inspection (FAI) reports per AS9102B, CMM dimensional inspection reports, surface finish certificates, heat treatment certificates, plating/anodizing certificates, and PPAP documentation (Levels 1–3) for automotive programs. All documents reference the specific lot number, purchase order, and drawing revision. Records are retained for a minimum of 10 years for aerospace and medical orders.
We requires a minimum Process Capability Index of Cpk ≥1.33 before production approval for any critical characteristic. This is equivalent to a defect rate below 64 parts per million (4σ) at the tolerance limits. For safety-critical or medical device applications, Cpk ≥1.67 (5σ, 0.6 ppm defect rate) is targeted. Out-of-control SPC signals trigger a production stop and root cause investigation before any potentially non-conforming parts are produced. Cpk data is available upon request for production programs.
Yes. Under GL Proto’s IATF 16949:2016 certification, PPAP documentation is available for Levels 1 through 3 per AIAG PPAP 4th Edition. Documentation includes Part Submission Warrant (PSW), dimensional results on sample parts, material certifications, process capability (Cpk) data, control plan, and PFMEA. Contact our engineering team at order placement to confirm PPAP requirements and documentation schedule — PPAP preparation is most efficient when initiated before first article production.
The quality protocol described on this page is not aspirational — it is the documented, audited system
that governed the production of Great Light 20,000+ delivered projects. When an aerospace buyer asks for
our AS9102 FAI capability or an automotive engineer asks for PPAP Level 3, the answer is the same:
yes, and we have done it before. Our three simultaneous ISO certifications exist because we serve
regulated supply chains simultaneously — and the documentation infrastructure required by each is
already in place, not built to order.
“Quality is not something we add to a part after it is machined.
It is what we build into the process before the first tool makes contact.”
— Mr. Bai, Senior Applications Engineer, Great Light
Every Great Light order ships with COC and MTR as standard. FAI, CMM report, PPAP, and full
documentation packages available on request. Submit your drawing — our engineering team
responds within 4–8 business hours.
ISO 9001 · IATF 16949 · ISO 13485 · No MOQ · In-house CMM · 10-year record retention
All uploads SSL-encrypted · NDA available · Certificate copies provided on request