For Small Brands & FBA Sellers

Pre-Launch QA Audit.
Senior Judgment.
One-Week Turnaround.

Independent quality engineering review of a consumer product before it ships. You send the spec sheet, supplier docs, and photos. We send back a risk-ranked report on what's likely to fail, why, and what to fix — in seven days.

20+ Years QA Experience
Federal Recall Data
Fixed Price · No Scope Creep
Standard Engagement
$1,500
Fixed price · 50% on engagement, 50% on delivery
★ Launch Offer · First 3 Audits
$750 — Half Price
For the first three engagements, in exchange for a written testimonial.
  • Written PDF report (10–15 pages)
  • Risk-ranked findings (high / medium / low)
  • 30-minute review call after delivery
  • One-week turnaround guaranteed
  • Senior QA engineer leading the work
Start an Engagement →
Who It's For

Built for brands without an in-house QA function

If you're shipping a consumer product to American homes and you've never had a senior quality engineer look at it, this audit is for you.

📦

Amazon FBA Sellers

Private-label brands launching new SKUs in regulated categories.

🛒

DTC Brands

Direct-to-consumer companies launching their first or second product line.

🚀

Crowdfunded Creators

Kickstarter and Indiegogo projects preparing for production fulfillment.

🏪

Small Manufacturers

Sub-$10M consumer goods firms without a dedicated QA hire.

The Process

What you send. What you get back.

One week from kickoff to delivered report. No discovery calls before scope is set, no surprise add-ons after.

You send

Five things, in any reasonable format

  1. Product spec sheet — whatever you have, even rough
  2. Supplier or manufacturer documentation (BOM, factory reports, certs)
  3. Photos of the prototype or production sample
  4. Links to two or three similar products already on market
  5. Your intended retail price and sales channels
You get back (1 week)

A written PDF report covering

  • 10-point quality audit — full breakdown against the published QA Audit methodology.
  • Risk-ranked findings — high / medium / low, with specific evidence and recommended actions.
  • Manufacturer reliability check — recall history and complaint patterns from CPSC / FDA / USDA / NHTSA.
  • Regulatory exposure flag — what compliance requirements apply, what's table stakes, what's missing.
  • Prioritized action list — fixes ranked by cost-to-fix vs. risk-reduction.
  • 30-minute review call — walk through findings, decide what to act on first.
What You Get

Six sections. One engineer-signed report.

The Pre-Launch QA Audit produces a written PDF with this exact spine. Every section is authored, reviewed, and signed off by the engineer on the byline.

SECTION 01

Top 5 Risks — Severity-Ranked

Each risk classified CRITICAL / MAJOR / MINOR / OBSERVATION. Specific failure mode named. Test standard or design control that catches it cited. Regulation tied per item.

SECTION 02

Comparable Recalls

Three to five most adjacent past recalls from the 20+ years of recall experience — daily-refreshed across CPSC, FDA, NHTSA, USDA, 20+ years. Each shown with recall number, units, hazard, root cause.

SECTION 03

Standards Stack

Which test standards apply. Which labs run them (ITS, UL, Bureau Veritas, TÜV). Typical turnaround windows. No invented prices — direct lookups against published lab catalogs.

SECTION 04

Pre-Tooling-Freeze Checklist

Decisions that must be locked before first production run. Each item tied back to a Top-5 risk so the founder knows what's optional and what's critical.

SECTION 05

Dollar Exposure Box

Two or three recent recalls in the CFORRS database with the disclosed dollar exposure: units recalled × disclosed retail = direct refund liability the manufacturer is now staring at.

SECTION 06

Next Step Card

Single recommended action. Either ship as-is with these caveats, run additional testing before tooling freeze, or revisit the supplier package. No vague "consider" language.

The Discipline Behind The Tool

Every report is built through a four-step engineer-led review.

The methodology structures an input against 20+ years of recall experience. An engineer reviews and leads every engagement, authoring every finding before delivery. That distinction is the entire point.

STEP 01

Extraction

Tooling structures the input — category, materials, energy source, use population, hazard class.

STEP 02

Confidence Flagging

Every field marked verified or unverified before any downstream logic runs. Nothing untrusted reaches the report.

STEP 03

Adjacency Check

Proprietary lookup against the 20+ years of quality and recall experience — CPSC, FDA, NHTSA, USDA, refreshed daily across 20+ years of recall history.

STEP 04

Engineer Sign-Off

No report ships without a named engineer leading the work. Tooling supports the labor; the engineer carries the verdict.

All four steps run on every paid Pre-Launch QA Audit. Engineer sign-off is non-negotiable. Tooling supports the data layer; the engineer carries the verdict and stands behind every finding.

Read the Full QA Audit Methodology →
Pricing

Fixed price. No hourly. No scope creep.

One number, paid half on engagement and half on delivery. The launch-offer rate applies to the first three engagements only.

Standard

Once the first three slots are filled.
$1,500
50% on engagement · 50% on delivery
  • Full 10-point QA Audit
  • Written PDF report
  • Risk-ranked findings + action list
  • Federal recall data check
  • 30-minute review call
  • 1-week turnaround
Email to Start →
Honest Scope

What this audit does NOT include

Knowing the limits is what makes the price fixed and the deliverable clean.

Out of scope

If any of the items below are what you actually need, the Pre-Launch QA Audit is not the right service. We'll tell you so before invoicing.

  • Physical product testing. We review documentation and field-data patterns. We do not destroy units on a test bench. Where physical testing would change the verdict, we say so.
  • In-person supplier or factory audits. Manufacturer track record is assessed via public regulatory data, not site visits.
  • Regulatory filings or submissions. We flag exposure and missing requirements. We do not handle FDA / CPSC / FCC / UL submissions on your behalf.
  • Post-launch monitoring. A separate service — Recall-Risk Monitor — is in development for ongoing category and product surveillance.
  • Litigation or expert-witness work. Available separately via direct engagement. Not part of this audit.
  • Anything missing from the documents you send. When information isn't there, we list what's missing — we do not invent assumptions to fill the gap.
The Unit Economics

Why this costs $1,500 instead of $30,000

A traditional senior quality consulting engagement runs twenty to fifty thousand dollars. Most pre-launch products don't need that depth — they need a senior eye on the obvious risks, delivered fast, at a price a seven-figure brand can actually pay.

🧭

The Engineer Authors the Work

What gets ranked high-risk, what's actually a recommendation versus a nice-to-have, what would never pass a real QA review — that's senior engineering judgment. Every finding, citation, and verdict is written and reviewed by us personally. One name leading the work.

⚙️

Tooling Accelerates the Data Layer

Federal recall pipelines, listing scrapes, and review aggregation move the data layer through faster than a junior consultant could — but every output is reviewed by the engineer before it informs a finding. Tooling supports the work; it does not substitute for the verdict.

📐

Fixed Scope, Fixed Price

No hourly billing. No discovery phase. No post-engagement scope creep. The deliverable is published in advance — you know exactly what you're paying for before the invoice goes out.

Who Runs the Audit

Senior QA engineer leading the work

One person owns every audit. No fictional staff. No rotating contractors. The name on the report is the name doing the work.

MM
About the Practitioner

Mark Mayeux

Quality Engineer · QESaaS

Twenty-plus years in product quality engineering across three categories where the cost of getting it wrong varies from ruined-your-Tuesday to ruined-your-life: medical devices, aerospace, and consumer goods. Same instinct, different stakes.

Directly relevant to this audit: Mark has personally performed supplier quality audits across medical consumables, medical devices, and consumer goods — he knows what to look for. He has led teams through years of ISO 9001, ISO 14001, and OHSAS 18001 certification audits, authoring company process documents and work instructions across every department. He also built the entire quality department at a medical equipment startup from scratch — hiring, agency documentation, supplier quality requirements, and supplier scoreboards — which was later acquired by a larger company.

Also the builder behind RecallSentry™, a published iOS and Android app that monitors federal recall feeds across CPSC, FDA, USDA, and NHTSA. The same daily-running data pipelines power the Pre-Launch QA Audit's manufacturer and category reliability data — and every output that lands in a paid deliverable is authored by Mark.

Quality & Six Sigma Regulatory Affairs Supplier Quality Auditing ISO 9001 / 14001 OHSAS 18001 Medical Devices Aerospace Automotive Consumer Products Med Equipment Startup → Acquisition Practitioner-Led Engagement
Common Questions

Before you email

The questions that come up most often.

How is this different from hiring a freelance QA consultant?

Freelance QA consulting typically bills hourly, requires a discovery phase, and takes 4–8 weeks per engagement. The Pre-Launch QA Audit is fixed price, fixed scope, fixed timeline — one week from kickoff to delivered PDF — because the methodology is published in advance and the federal-data and review-aggregation tooling moves the data layer through faster than a junior consultant could. The engineer still reviews and leads every finding before delivery.

Will you sign an NDA?

Yes. A mutual NDA can be signed before you send any product documents. We have a one-page template that covers most cases; if you have your own, that's fine too.

What if my product is in a category you've never reviewed?

The 10-point methodology is category-agnostic. The federal-data lookup adapts to your product's regulatory category (CPSC, FDA, USDA, or NHTSA, depending on what you're shipping). If your category has unusual requirements that fall outside the published scope, we'll tell you on the first email exchange — not after invoicing.

Do you guarantee my product won't get recalled?

No quality engineering review can guarantee that. What we guarantee is that the obvious failure modes, the manufacturer track-record red flags, and the regulatory exposure issues that would be visible in your documents and the public data will be in the report. What you do with the findings is your call.

What if I don't have all five inputs?

Send what you have. The first thing the report does is list what's missing — that's part of the value. If too much is missing for a useful audit, we'll tell you before invoicing rather than after.

Do you do international products?

The federal-data layer covers U.S. regulatory exposure — CPSC, FDA, USDA, NHTSA. If you're selling internationally and U.S. compliance isn't your primary concern, this audit is a partial fit at best. Email and we'll tell you whether it's worth the engagement.

Ready to run the audit?

Book a free 30-minute scoping call to walk through what you're launching. If it's a fit, you'll get a one-page engagement brief and an invoice. If it's not, we'll tell you why.