Identification
Item/part numbers, revision level, drawing reference, purchase order, and lot/serial numbers to precisely identify the sample under inspection.
A Business FAI Document centralizes inspection evidence, reduces rework by documenting deviations and corrective actions, and establishes an auditable acceptance trail for contracts, supplier management, and regulatory reviews.
Personnel who prepare or review the Business FAI Document include quality engineers, inspectors, suppliers, procurement, and receiving departments.
Auditors, contract managers, and manufacturing engineers also reference the document to support dispute resolution and continuous improvement.
Item/part numbers, revision level, drawing reference, purchase order, and lot/serial numbers to precisely identify the sample under inspection.
Measured dimensions with tolerances, methods used, instruments, individual readings, and pass/fail status for each characteristic inspected.
Descriptions of test procedures, acceptance criteria, environmental conditions, and links to calibration or test reports supporting the results.
Detailed descriptions of deviations, severity classification, photos or attachments, and immediate containment actions taken by supplier or inspector.
Root cause analysis, corrective action plan, owner, due dates, and verification steps showing how the issue was resolved or mitigated.
Sign-off lines for supplier, inspector, quality lead, and buyer with printed name, title, date, and traceable signature method.
| Field | Configuration |
|---|---|
| Required Fields | Make part number, measurements, and signature blocks mandatory. |
| Conditional Logic | Show corrective action blocks only when nonconformity is flagged. |
| Signer Order | Route supplier → inspector → buyer in sequential order. |
| Notifications | Enable email and SMS reminders for pending approvals. |
Choose a platform that supports secure signatures, audit trails, and your required integrations for traceability and storage.
Commonly 7–30 days from delivery or production sample availability.
Suppliers often have 10–30 business days to propose corrective actions.
Buyers typically review and respond within 5–15 business days.
Finalized FAIs should be filed within project document control timelines.
Reinspection schedules depend on corrective action verification and contractual terms.
Customer or engineering requests first article sample for inspection.
Supplier logs receipt and assigns identification for the sample.
Measurements and tests are executed and recorded with evidence.
Buyer issues formal acceptance or requests corrective actions.
| signNow | DocuSign | Adobe Sign | PandaDoc | HelloSign | |
|---|---|---|---|---|---|
| Starting Price | $8/user/mo | $15/user/mo | $14/user/mo | $19/user/mo | $15/user/mo |
| Free Trial | 7-day free trial | Varies by plan | Varies by plan | Varies by plan | Varies by plan |
| Bulk Send | Yes | Yes | Yes | Yes | No |
| Audit Trail | Yes | Yes | Yes | Yes | Yes |
| HIPAA Compliant | Yes | Yes | Yes | No | No |
Tim Martin streamlined inspections and approvals online to avoid in-person signings.
BIS selected a secure signing platform to centralize acceptance records and audit trails.
The Quality Lead reviews measurement data, confirms acceptance criteria are met, and provides final sign-off. They coordinate corrective action verification and ensure the FAI links to related quality records for audits and supplier performance tracking.
The Supplier Representative completes the report, supplies test certificates, and certifies production readiness. Their signature attributes responsibility and triggers buyer inspection or release procedures according to contractual terms.