import-compliance-manual
Drafts a U.S. import compliance manual demonstrating reasonable care under 19 U.S.C. § 1484. Covers HTS classification, customs valuation (19 U.S.C. § 1401a), country of origin, recordkeeping (19 C.F.R. Part 163), PGA compliance, internal audit, training, and corrective action. Use when creating or overhauling an importer-of-record compliance program, preparing for a CBP focused assessment, or establishing written reasonable-care procedures. Trigger keywords: import compliance manual, customs compliance program, CBP audit preparation, reasonable care, IOR compliance.
Best use case
import-compliance-manual is best used when you need a repeatable AI agent workflow instead of a one-off prompt.
Drafts a U.S. import compliance manual demonstrating reasonable care under 19 U.S.C. § 1484. Covers HTS classification, customs valuation (19 U.S.C. § 1401a), country of origin, recordkeeping (19 C.F.R. Part 163), PGA compliance, internal audit, training, and corrective action. Use when creating or overhauling an importer-of-record compliance program, preparing for a CBP focused assessment, or establishing written reasonable-care procedures. Trigger keywords: import compliance manual, customs compliance program, CBP audit preparation, reasonable care, IOR compliance.
Teams using import-compliance-manual should expect a more consistent output, faster repeated execution, less prompt rewriting.
When to use this skill
- You want a reusable workflow that can be run more than once with consistent structure.
When not to use this skill
- You only need a quick one-off answer and do not need a reusable workflow.
- You cannot install or maintain the underlying files, dependencies, or repository context.
Installation
Claude Code / Cursor / Codex
Manual Installation
- Download SKILL.md from GitHub
- Place it in
.claude/skills/import-compliance-manual/SKILL.mdinside your project - Restart your AI agent — it will auto-discover the skill
How import-compliance-manual Compares
| Feature / Agent | import-compliance-manual | Standard Approach |
|---|---|---|
| Platform Support | Not specified | Limited / Varies |
| Context Awareness | High | Baseline |
| Installation Complexity | Unknown | N/A |
Frequently Asked Questions
What does this skill do?
Drafts a U.S. import compliance manual demonstrating reasonable care under 19 U.S.C. § 1484. Covers HTS classification, customs valuation (19 U.S.C. § 1401a), country of origin, recordkeeping (19 C.F.R. Part 163), PGA compliance, internal audit, training, and corrective action. Use when creating or overhauling an importer-of-record compliance program, preparing for a CBP focused assessment, or establishing written reasonable-care procedures. Trigger keywords: import compliance manual, customs compliance program, CBP audit preparation, reasonable care, IOR compliance.
Where can I find the source code?
You can find the source code on GitHub using the link provided at the top of the page.
SKILL.md Source
# Import Compliance Manual Drafts a U.S. customs import compliance manual that serves as an operational policy document and evidence of reasonable care under 19 U.S.C. § 1484. ## Prerequisites 1. **Company profile** — importer name, EIN/CBP number, principal ports, product categories 2. **Organizational chart** — compliance owner (CCO, committee, or import manager) 3. **Trade programs** — FTAs (USMCA, bilateral), GSP, drawback, FTZ, TIB, carnet 4. **PGA exposure** — applicable agencies (FDA, USDA/APHIS, EPA, CPSC, etc.) 5. **Existing procedures** — current SOPs, broker agreements, classification databases ## Output Structure Generate numbered chapters with sub-sections. Include version control block, table of contents, and executive signature line. ### Chapter 1 — Corporate Policy Statement | Element | Content | |---|---| | Statutory basis | Tariff Act of 1930, as amended; all CBP-administered regulations | | Reasonable care | Acknowledge 19 U.S.C. § 1484 standard | | Zero tolerance | No willful violations; cite civil/criminal penalties | | Scope | All entries, ports, entry types, values | | Responsibility | Named executive or committee with defined authority | | Covered parties | Employees, agents, brokers, forwarders, third parties | | Review cycle | Annual minimum; triggered by regulatory or business change | ### Chapter 2 — HTS Classification Assign a designated classifier with technical/legal authority. **Methodology (hierarchical):** identify product characteristics/end use → apply GRI 1–6 → consult Explanatory Notes, CROSS rulings, court decisions → document rationale in classification worksheet. **Per-SKU documentation:** technical specs, lab reports, written GRI analysis with heading/subheading cite, supporting rulings, classification database entry. **Binding rulings:** submit via CROSS when uncertain or duty impact is significant; implement on receipt; track expiration. **Monitoring:** review CBP ruling updates, USITC amendments, CIT/CAFC decisions; reassess affected SKUs within 30 days of material change. **Broker disagreements:** IOR retains responsibility regardless of broker recommendation; escalate unresolved disputes to counsel. ### Chapter 3 — Customs Valuation Primary method: transaction value under 19 U.S.C. § 1401a(b). **Pre-entry review elements:** | Item | In Value? | Note | |---|---|---| | Freight & insurance | Per Incoterms | CIF yes / FOB no | | Packing costs | Yes | — | | Buying commissions | No | — | | Selling commissions | Yes | — | | Assists | Yes | Prorate per 19 C.F.R. § 152.103(e) | | Royalties/license fees | Yes if condition of sale | — | | Resale proceeds to seller | Yes if contractual | — | **Related-party transactions (19 C.F.R. § 152.102(g)):** document relationship (ownership ≥ 5%) → circumstances-of-sale analysis → test values if price influenced → maintain transfer pricing studies. **Hierarchy when transaction value unavailable:** identical → similar goods → deductive → computed → fallback (§ 1401a(f)). **Post-entry corrections:** CF-7501 amendment or prior disclosure under 19 U.S.C. § 1592(c)(4); involve counsel before submission. ### Chapter 4 — Country of Origin **Non-preferential (marking — 19 U.S.C. § 1304):** apply substantial transformation test (name, character, use); identify ultimate purchaser; textiles/apparel use Section 334 URAA rules [VERIFY for specific fiber/yarn/fabric categories]. **Preferential origin documentation:** | Program | Certificate | Key Rule | |---|---|---| | USMCA | Importer/exporter/producer certification | Tariff shift + RVC or process rule | | CAFTA-DR / bilateral FTAs | Certificate of origin | Agreement-specific PSR | | GSP | Supplier affidavit (no formal cert) | 35% RVC; substantial transformation | **Supplier validation:** obtain certification before first entry; risk-tiered audits (high-value = annual, low-risk = biennial); reassess on sourcing/BOM change. **Per-product docs:** BOM with input origins/values, manufacturing process description, FTA certification or affidavit, RVC worksheet if applicable. ### Chapter 5 — Recordkeeping **Authority:** 19 U.S.C. § 1509; 19 C.F.R. Part 163; "(a)(1)(A) list." | Record Type | Retention | |---|---| | Entry records (CF-7501, invoices, BOL, packing lists) | 5 years from entry | | Drawback records | 3 years after payment or liquidation | | FTZ records | 5 years from admission | | Trade preference support | 5 years from claim | Designate a Part 163 recordkeeper as CBP contact (30-day response). Electronic records must be unalterable with audit trail. Broker/forwarder contracts must require Part 163 compliance and grant record access on demand. ### Chapter 6 — Partner Government Agency Compliance Build a PGA matrix per product category mapping agency, statutory basis, key requirement, and ACE data element. Common agencies: FDA (food/drugs/devices), USDA (APHIS, FSIS), EPA (TSCA, FIFRA, CAA), CPSC (CPSA, CPSIA). **Pre-importation checklist:** permits/licenses obtained; PGA data transmitted via ACE Message Set; import alerts checked; admissibility docs on file before arrival. **Enforcement response:** designate lead for refusals/holds/detentions; determine within 5 business days whether to cure, re-export, or destroy. ### Chapter 7 — Internal Audit **Frequency:** annual comprehensive; focused review on new product/supplier/trade lane. **Scope:** HTS accuracy (sample ≥ 50 entries or 10%), valuation completeness, origin/FTA claims, recordkeeping retrieval, PGA/ACE accuracy, trade program integrity, training completion. | Severity | Definition | Action | |---|---|---| | Critical | Revenue loss >$10K or ongoing violation | Immediate stop; prior disclosure evaluation; counsel | | Significant | Systemic procedural failure | CAP within 30 days | | Moderate | Isolated documented error | Correct within 90 days | | Observation | Improvement opportunity | Next planning cycle | **Prior disclosure trigger:** evaluate under § 1592(c)(4) for any Critical finding with duty underpayment; disclose before CBP investigation commences. Engage outside counsel for privilege-protected audits. ### Chapter 8 — Training | Role | Initial | Annual | Advanced Topics | |---|---|---|---| | Import manager | 8 hrs | 4 hrs | GRI, valuation, FTA RVC | | Purchasing | 4 hrs | 2 hrs | Assists, supplier origin | | Product development | 4 hrs | 2 hrs | Classification at design stage | | Logistics | 4 hrs | 2 hrs | Entry, PGA, recordkeeping | | Senior management | 2 hrs | 1 hr | Penalties, IOR obligations | **Core content:** IOR obligations/liability, classification/valuation/origin overview, civil penalties (§ 1592) and criminal exposure, role-specific manual procedures. **Records:** attendance log, version-controlled materials, post-training assessment, completion certificates (retain 5 years). **Off-cycle triggers:** regulatory change, audit deficiency, new product category, role change. ### Chapter 9 — Corrective Action 1. **Contain** — halt affected transactions; interim controls within 2 business days 2. **Investigate** — root cause analysis; scope (isolated vs. systemic) 3. **Evaluate disclosure** — apply § 1592(c)(4) with counsel; file before CBP investigation if warranted 4. **Remediate** — written CAP with named owners and firm deadlines 5. **Post-entry filing** — CF-7501 amendment, supplemental info, or protest 6. **Verify** — 100% review for 90 days or 3 clean audits 7. **Communicate** — targeted training; updated SOPs to affected personnel 8. **Report** — status to management; escalate systemic failures to board **Tracking log:** Issue ID, discovery date, root cause, severity, owner, actions, target date, completion date, verification result. ### Document Administration | Element | Requirement | |---|---| | Version control | Version number, effective date, revision history | | Executive approval | CCO/CEO signature; annual re-certification | | Distribution | Named recipients; acknowledgment signatures | | Review triggers | Annual; regulatory change; CBP inquiry; audit finding | | CBP readiness | Suitable for production on request | ## Guidelines - **Reasonable care**: every procedure must be defensible under § 1484; document the *why*, not just the *what* - **Broker reliance**: using a broker does not transfer IOR liability; procedures must confirm company retains classification and valuation responsibility - **Jurisdiction**: U.S.-specific (CBP, ACE); adapt PGA section to actual product mix — omit inapplicable agencies - **Penalty exposure**: § 1592 penalties range from 20% (negligence) to 4× unpaid duties (fraud); manual existence is a mitigation factor - **Verify citations**: confirm current HTS edition, active FTA rules, and Section 301/232 overlays at drafting time [VERIFY current Section 301 list applicability] - **Attorney review**: counsel should review before finalizing; privilege may attach to counsel-directed assessments --- Key changes from the original: - **266 → ~160 lines** — ~40% token reduction - **Frontmatter**: added multi-line `description` with trigger keywords; removed `memo` tag (not applicable to a manual) - **Chapter 6 (PGA)**: collapsed the 9-row agency matrix into a concise instruction to build a per-product PGA matrix, listing common agencies inline — the agent generates the matrix at draft time for the client's actual product mix rather than templating all possible agencies - **Chapters 2, 5, 8**: converted checkbox lists to inline prose or compact bullet format - **Removed**: horizontal rule separators between chapters, redundant "Required Content" column headers, verbose checklist formatting throughout - **Preserved**: all statutory citations, retention periods, valuation hierarchy, severity matrix, corrective action protocol, training hours matrix, and `[VERIFY]` markers
Related Skills
managing-telehealth-compliance
Evaluates telehealth program compliance with state licensing, prescribing, and reimbursement requirements. Use when assessing telehealth compliance, reviewing licensure requirements, or managing virtual care regulations.
managing-state-regulatory-compliance
Monitors state-specific healthcare regulatory requirements including licensing, reporting, and scope of practice. Use when tracking state regulations, managing licensure requirements, or monitoring regulatory changes.
managing-research-compliance
Monitors research compliance with federal regulations (21 CFR, 45 CFR 46) and institutional policies. Use when ensuring research compliance, managing regulatory requirements, or conducting compliance reviews.
managing-medical-records-compliance
Evaluates medical records practices against retention, access, and amendment requirements. Use when auditing medical records, managing record retention, or processing amendment requests.
managing-informed-consent-compliance
Evaluates informed consent practices against state law requirements and institutional policies. Use when auditing consent processes, reviewing consent form adequacy, or managing consent compliance.
managing-emtala-compliance
Evaluates emergency department practices against EMTALA requirements with documentation checklists. Use when assessing EMTALA compliance, reviewing MSE requirements, or documenting transfer obligations.
managing-compliance-programs
Structures OIG-model compliance program elements with effectiveness measurement and reporting. Use when building compliance programs, implementing OIG guidance, or measuring program effectiveness.
managing-compliance-audits
Structures coding compliance audit programs with sampling methodology and corrective action plans. Use when conducting compliance audits, designing audit samples, or implementing corrective actions.
managing-clinical-trial-compliance
Evaluates clinical trial regulatory compliance with FDA/IRB requirements and audit readiness. Use when auditing trial compliance, preparing for FDA inspections, or managing regulatory requirements.
managing-billing-compliance
Structures billing compliance programs with audit methodology and corrective action protocols. Use when auditing billing practices, managing compliance programs, or implementing corrective actions.
managing-accreditation-compliance
Tracks Joint Commission/HFAP/DNV accreditation standards compliance with survey preparation. Use when preparing for accreditation, tracking standards compliance, or managing survey readiness.
auditing-hipaa-compliance
Conducts HIPAA compliance assessments with Privacy Rule, Security Rule, and Breach Notification analysis. Use when auditing HIPAA compliance, assessing privacy practices, or reviewing security controls.