skills/legal/import-compliance-manual/SKILL.md
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.
npx skillsauth add casemark/skills import-compliance-manualInstall this skill globally with one command. Works with Claude Code, Cursor, and Windsurf.
3 of 9 scanners reported clean
Some scanners were skipped, did not run, or reported a non-clean status. Review each row below.
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.
Generate numbered chapters with sub-sections. Include version control block, table of contents, and executive signature line.
| 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 |
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.
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.
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.
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.
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.
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.
| 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.
Tracking log: Issue ID, discovery date, root cause, severity, owner, actions, target date, completion date, verification result.
| 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 |
Key changes from the original:
description with trigger keywords; removed memo tag (not applicable to a manual)[VERIFY] markerstools
Audits the complete in-scope medical-record universe in a litigation matter and produces an attorney-facing, Bates-cited analysis of treatment gaps, missing records or providers, baseline coverage, material billing or production mismatches, and complaint evolution. Use when asked to find missing medical records, analyze treatment gaps or first-care timing, identify absent providers, assess whether a production is complete, or prepare a records-request target list. Use medical-record-chronology instead when the primary request is a chronological clinical narrative.
development
Drafts a legally compliant Private Placement Memorandum for Regulation D offerings (Rule 506(b)/506(c)), covering full disclosure framework including risk factors, capitalization, securities terms, use of proceeds, and investor qualification requirements. Enforces SEC anti-fraud compliance under Section 10(b)/Rule 10b-5, blue sky law considerations, and accredited investor verification under Rule 501. Use this skill when drafting PPMs, offering memorandums, Reg D disclosure documents, or private offering circulars for issuers raising capital from sophisticated investors. Also trigger when the user mentions private placement disclosure, offering memorandum, Reg D fundraising, or accredited investor verification. Even if the user just says "PPM" or "draft our offering memo," use this skill.
data-ai
Generates structured privacy and data protection law briefings across US, EU, UK, and other jurisdictions. Organizes by jurisdiction with compliance deadlines, enforcement actions, and legislative changes. Use when preparing privacy law briefings, compliance updates, regulatory change summaries, or data protection landscape reviews.
testing
Generates structured summaries of prior art references for patent prosecution, validity analysis, and freedom-to-operate assessments. Maps disclosures to claim elements with precise citations. Use when summarizing prior art, analyzing patent landscapes, mapping references to claims, or preparing office action responses.