Industry sourcing guide

Supplier Factory-Audit & Capability Verification Guide

For buyers of lithium-PACK and industrial drone products: breaking a factory audit into three levels — document review, remote video and on-site inspection — covering qualification systems, capacity and equipment, incoming and in-process quality, cell sourcing and traceability, and export-compliance readiness, with an executable checklist that front-loads quality and delivery risk to the RFQ stage.

01Why audit: front-load the risk

Sourcing risk is not only price but the gap between what is promised and what is done: samples pass yet mass production drifts, capacity gets crowded out by larger customers and lead times slip, or a missing quality system causes batch-to-batch inconsistency. A factory audit is about answering three questions with verifiable evidence: does this factory really exist with real capacity in this category, can it repeatedly reproduce sample quality, and does it understand the compliance and market-access rules of your target market. Confirming these at RFQ and sampling stage is far cheaper than fixing problems after mass production.

  • Does it really exist with real capacity in this category
  • Can it repeatedly reproduce sample quality
  • Does it understand target-market compliance and access

02Three levels: document / remote / on-site

Not every purchase needs an on-site visit. In increasing order of effort there are three levels: document review (business licence, system certificates, test reports, capacity and equipment lists — cheapest, fully remote), remote video audit (a live walk-through of lines, warehouse and test lab along a preset route, with timestamps and workstation footage), and on-site inspection (a third party or your own staff checking documents against physical reality and interviewing key roles). Screen out obvious mismatches with document review first, then run remote or on-site audits on the shortlist so effort concentrates on the few suppliers you will actually order from.

  • Document review: cheapest, fully remote
  • Remote video: live walk-through along a preset route
  • On-site: cross-check documents against physical reality

03Qualification and system documents

Document review should request material that can be cross-checked: legal entity (business licence, whether the scope covers the category), quality and environmental systems (ISO 9001 and, where applicable, IATF 16949), product certifications and test reports (per target market), and capacity and equipment lists. The key is cross-verification: does the licence address match the site or video, is the certificate valid and does its scope cover this product line, does the test report model match the quoted model. For lithium products also examine cell sourcing and datasheets.

  • Licence address matches site or video
  • Certificate valid and scope covers this line
  • Test-report model matches the quoted model

04Capacity and equipment verification

Capacity is not a single number but whether your order can be scheduled within the given lead time. Check the equipment list and how much of the key process is in-house (own lines vs outsourced relabelling), the count and models of key equipment, actual shifts and work-in-progress, and the current load; ask for recent schedules or shipment records as corroboration. For categories involving cell matching, such as lithium and drones, also confirm whether sorting and matching equipment and ageing / charge-discharge test equipment are in-house — this directly determines mass-production consistency and is where a relabelling factory is most likely to be exposed.

  • Key process in-house vs outsourced relabelling
  • Sorting / matching and ageing test equipment in-house
  • Current load and achievable lead time

05Quality and consistency: IQC / IPQC / OQC

Quality must land in three stages: incoming inspection (IQC, especially the acceptance criteria and non-conformance handling for cells, BMS and structural parts), in-process inspection (IPQC, patrol and records at key steps such as welding, spot-welding, assembly and potting), and outgoing inspection (OQC, sampling ratio, ageing and full-test items). Request recent sample inspection records and the non-conforming-material process, and confirm batch traceability — whether a finished batch can be traced back to cell batches and test data. Whether records are continuous and signed and dated tells you more about real management than the certificate itself.

  • IQC acceptance criteria and non-conformance handling
  • IPQC patrol records at key steps
  • OQC sampling ratio and batch traceability

06Battery and drone-specific checks

For lithium products verify: cell sourcing and whether it is an authorised channel, the sorting and matching standard (capacity / internal-resistance / voltage binning accuracy) and consistency data, BMS protection parameters and balancing strategy, and test data (cycle, rate, low temperature, and safety items such as nail penetration and overcharge). For complete industrial drones verify: the sourcing and self-development share of the flight controller and key parts (motors, radar, blades), complete-aircraft test and flight records, and the substitutability of critical parts (to avoid a single point of supply failure). These determine post-production reliability and after-sales cost — sample specs alone are not enough.

  • Cell sourcing and sorting / matching accuracy
  • BMS protection parameters and balancing strategy
  • Flight-controller and key-part sourcing, substitutability

07Front-load compliance and export readiness

Use the audit to bring compliance forward: for an EU target, confirm the factory’s understanding of and documentation for the EU Battery Regulation (including battery passport and carbon-footprint requirements); for complete-drone exports, confirm the target market’s aircraft access and certification requirements; shipping lithium batteries is a dangerous-goods exercise, so confirm the factory can supply a UN38.3 test summary, MSDS and compliant packaging. State the target country and use case in the RFQ so the platform can flag the relevant compliance points — assessing landed cost during comparison instead of discovering missing documents once goods are ready.

  • EU Battery Regulation documentation readiness
  • Target-market aircraft access and certification
  • UN38.3 / MSDS / dangerous-goods packaging

08Remote audit checklist (when on-site is impossible)

When on-site is impossible, substitute a structured remote audit: pre-set the video route (raw-material store → cell store → production line → ageing and test area → finished-goods store → QC lab), require real-time, unedited footage with close-ups at key workstations; spot-check original documents (licence, certificates, recent inspection records) for validity and model; witness one key test remotely (e.g. charge-discharge or leak test); and request extra documents or third-party reports for doubtful items. Write the conclusion into a formal record and file it in the supplier profile as the basis for re-audits and comparison, instead of asking the same questions again each time.

  • Preset route, real-time and unedited
  • Spot-check original documents for validity and model
  • Witness one key test remotely

Related compliance & market access

EU battery passport

2026-08-11Requirement

Basis:GBA battery passport pilot; EU passport compliance cascades to upstream Li-ion supply chain since 2026-08-11.

Platform action:Factory must declare "battery passport compliant" and provide traceability data.

EU Battery Regulation

2026-06-30Requirement

Basis:EU Battery Regulation: carbon footprint, recycled-content, battery passport, EPR (2026 EU green supply-chain compliance report, 2026-06-30).

Platform action:Provide compliance declaration, carbon footprint and third-party test reports.

Airworthiness (TC/PC/AC/OC)

2024-04-07Requirement

Basis:Airworthiness chain: TC/PC/AC/OC; EHang EH216-S received the world’s first manned eVTOL PC on 2024-04-07 (Zheshang Securities 2024-04-09).

Platform action:Airframes / eVTOL must hold corresponding airworthiness certificates, surfaced on factory detail.

FAQ

Do I always need an on-site audit?

No. Start with document review (cheapest, fully remote) to screen out obvious mismatches, then run remote video audits on the shortlist; only when the order value is large, the category risk high (e.g. power or ESS batteries) or a long-term relationship is intended is a third-party or in-house on-site audit worth arranging. The three levels combine, concentrating effort on the few suppliers you will actually order from.

How do I know a certificate or report is trustworthy?

Verify by number on the issuing body’s website or an accreditation platform, checking entity name, address, validity and whether the certification scope covers the target product line. For test reports, check the product model, test items and standard version against the quoted model. Where needed, ask the issuing or testing body for written confirmation. A certificate alone does not prove capability — combine it with inspection records and on-site or video verification.

Can I trust the capacity figures?

A single number is not trustworthy — cross-verify with evidence: the equipment list and how much of the key process is in-house, actual shifts and work-in-progress, recent schedules and shipment records, and whether critical equipment such as sorting / matching and ageing test lines are owned. Relabelling factories typically trip up on the “key process in-house” item. If the lead time is tight, also confirm the current load and whether your order can be scheduled.

What if the cells are not from an authorised channel?

Ask for cell datasheets, batch data and a sourcing statement, and write the cell source, substitution rules and liability split into the contract. Unauthorised channels bring consistency variance and liability risk, especially in power and ESS applications. If the source cannot be confirmed, require an authorised channel in the RFQ and treat it as a hard condition of supplier verification.

How long does an audit take and what does it cost?

It depends on the level: document review typically takes 1–3 days at near-zero cost; a remote video audit about half a day to a day, mainly coordination time; an on-site audit via a third party is billed per person-day plus travel and needs booking ahead. Choose the level by order size and category risk rather than running the heaviest audit on every candidate.

How do I verify suppliers on CellFlight?

Platform-verified suppliers carry a verification status and growth score; their profiles show main categories, location and public information, and you can request L2/L3 specs on product pages for side-by-side comparison. When posting an RFQ you can state whether an audit is required and which evidence you need (system certificates, test reports, inspection records, sourcing statements); the platform flags the relevant compliance points by target market so you can convey verification requirements to multiple factories at once.

Start sourcing

Post a structured RFQ; the platform auto-matches verified factories by application and target market, and returns a compliance and risk summary.

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