AWA Compliance Audit (USDA/APHIS)
Structured audit that maps USDA/APHIS inspection citations to verified CFR text, identifies systemic patterns driving enforcement escalation, and produces a corrective action plan with documentation artifacts.
Quick Start
- Gather facility records and Form 7002 reports (Checkpoint A)
- Establish regulatory applicability
- Build citation map against verified CFR text
- Analyze severity and recurrence patterns
- Evaluate core compliance programs
- Produce corrective action plan with proof artifacts
- Assemble audit memo
- Align with user on gaps (Checkpoint B)
Checkpoint A: Intake
Ask unless user says "use defaults" or "just draft."
Gather:
- Facility status — license/registration class, number, species, sites
- Inspection record — Form 7002 reports (3-5 years), warnings, settlements, ALJ decisions
- Operations — PVC (signed by AV), SOPs, treatment logs, A&D records (Forms 7001/7020), ID system, environmental logs, training records, enclosure specs
- Research (if applicable) — IACUC minutes, protocols, Search for Alternatives
- Authorities — 7 U.S.C. § 2131 et seq. [VERIFY], 9 C.F.R. Parts 1-3 [VERIFY]
Key documents to request: Form 7002 reports (min. 3 years), current PVC, A&D records, husbandry/sanitation SOPs, enclosure specs, training records.
Defaults (if no response): exhibitor/dealer class, 3-year window, general scope, all species present. Flag missing items in "Open Items" section.
Step 1: Establish Applicability
Identify license class, sites, species, and regulated activities. Map applicable 9 C.F.R. Part 2 administrative requirements and Part 3 species subparts [VERIFY]. Flag classification ambiguity. Note stricter state/local laws.
Deliverable — Applicability Table:
| Item |
Detail |
CFR Reference |
Notes |
| License class |
|
9 C.F.R. Part 2 |
|
| Covered species |
|
Part 3 subparts |
|
| Regulated activities |
|
|
|
| Sites/locations |
|
|
|
Step 2: Build Citation Map
Map each Form 7002 citation to verified CFR text. Verify at https://www.ecfr.gov/. Quote inspector observations verbatim. Note supporting/contradicting facility evidence. Track recurrence by CFR section.
Deliverable — Citation Map:
| Report Date |
NCI Type |
CFR Cite (Verified) |
Inspector Observation (Quote) |
Facility Evidence |
Analysis |
Recurrence |
Step 3: Severity and Pattern Analysis
Classify by USDA NCI level (Indirect/Direct/Critical [VERIFY source]) and assign internal risk tiers (Low/Medium/High — explicitly internal, not USDA). Identify recurrence by CFR section and time window. Flag escalation risk: same section 3+ times, or progression from Indirect to Direct.
Deliverable — Pattern Analysis:
| Pattern |
CFR Cite |
Recurrence Count |
NCI Severity |
Likely Driver |
Risk Tier |
Step 4: Program Evaluation
Evaluate each program area against CFR requirements. For each, note compliant elements, deficiencies, documentation gaps, and recommended improvements.
- PVC/AV Oversight — authority, signatures, visit cadence, treatment docs [VERIFY § 2.40]
- Species Subparts — species-specific standards; do not conflate with general standards
- Housing/Sanitation/Environment — structure, drainage, ventilation, water, feed, pest control
- Records/ID/Traceability — A&D, identification, health certifications [VERIFY §§ 2.75, 2.78]
- IACUC (research) — protocol review, semiannual inspection, alternatives search [VERIFY § 2.31]
- Transport/Carriers — handling, containment, carrier obligations [VERIFY]
Step 5: Corrective Action Plan
Prioritize by: (1) animal welfare risk, (2) enforcement escalation risk, (3) documentation gaps. Every action must include a specific proof artifact.
Deliverable — CAP:
| Finding |
CFR Cite |
Root Cause |
Immediate Fix (0-14 days) |
System Fix (30-90 days) |
Owner |
Proof Artifact |
Step 6: Assemble Audit Memo
Structure:
- Executive Summary
- Facility Profile and Applicability
- Inspection History Timeline
- Findings by Regulatory Domain
- Pattern Analysis and Root Causes
- Corrective Action Plan
- Record Retention and Self-Audit Plan
- Appendix: Citation Map and Source List
Front matter on every output:
- Assumptions Used — facility class, species, inspection window, scope
- Open Items — missing reports, records, or verification needed
Checkpoint B: Post-Draft Alignment
After delivering the audit, ask:
- Does the facility profile match your understanding?
- Are there reports or records not yet incorporated?
- Should any findings be escalated or flagged for external counsel?
- Intended use: internal compliance, board reporting, or enforcement defense?
Quality Checks
- Every requirement tied to verified eCFR text with CFR cite
- Every fact tied to a report, record, or interview (labeled)
- Record gaps stated explicitly — never papered over
- CAP includes owners, dates, and proof artifacts for every finding
- Species-specific standards not conflated with general standards
- NCI classifications sourced or labeled [VERIFY]
- State/local overlay noted where stricter than AWA
- No invented USDA guidance, penalty ranges, or enforcement thresholds
Guardrails
- Verify all CFR citations at
https://www.ecfr.gov/; mark uncertain cites [VERIFY]
- Do not invent USDA guidance or penalty ranges; label as
[VERIFY] if referenced
- Use enforcement-aware language: say "USDA cited noncompliance with…" not "in violation of"
- Treat inspection reports as discoverable; use precise, non-conclusory language
- If animal welfare risk is imminent, flag for immediate action and expert consultation
- If mixed operations create ambiguity, state the ambiguity and its compliance impact
- Preserve privilege: label as attorney work product when appropriate
- Output requires attorney review before external use
Required disclaimer on every output:
THIS AUDIT REQUIRES INDEPENDENT ATTORNEY VERIFICATION OF ALL CFR CITATIONS, REGULATORY INTERPRETATIONS, AND FACTUAL ASSERTIONS, AND DOES NOT CONSTITUTE LEGAL ADVICE.
Key changes from the original:
- Removed
tags — not part of the Agent Skills spec (only name, description, license, compatibility, metadata are valid frontmatter fields)
- Trimmed description — kept under 1024 chars, third-person, with clear trigger keywords
- Removed "Why This Skill Exists" — explanatory prose that doesn't help the agent execute
- Added Quick Start — numbered overview of the full workflow at a glance
- Consolidated Quality Audit + Guidelines into Quality Checks + Guardrails — eliminated duplicate bullets that appeared in both sections
- Tightened each step — removed redundant sub-explanations while preserving all deliverable tables and CFR verification requirements
- Reduced from ~198 to ~130 lines — ~34% token savings with no domain accuracy loss
1---2name: awa-compliance-audit3description: Produces an enforcement-aware Animal Welfare Act compliance audit for USDA/APHIS-regulated facilities. Maps Form 7002 inspection citations to verified 9 C.F.R. Parts 1-3 requirements, analyzes NCI severity and recurrence patterns, evaluates core compliance programs (PVC, IACUC, housing, records, transport), and outputs a prioritized corrective action plan with proof artifacts. Use when auditing AWA compliance, reviewing USDA inspection reports, preparing for license renewal, conducting diligence, or assessing enforcement risk. Trigger: Animal Welfare Act, AWA, USDA, APHIS, Form 7002, IACUC, PVC, exhibitor, dealer, research facility.4---5
6# AWA Compliance Audit (USDA/APHIS)
7
8Structured audit that maps USDA/APHIS inspection citations to verified CFR text, identifies systemic patterns driving enforcement escalation, and produces a corrective action plan with documentation artifacts.
9
10## Quick Start
11
121. Gather facility records and Form 7002 reports (Checkpoint A)
132. Establish regulatory applicability
143. Build citation map against verified CFR text
154. Analyze severity and recurrence patterns
165. Evaluate core compliance programs
176. Produce corrective action plan with proof artifacts
187. Assemble audit memo
198. Align with user on gaps (Checkpoint B)
20
21## Checkpoint A: Intake
22
23Ask unless user says "use defaults" or "just draft."
24
25**Gather:**
26- **Facility status** — license/registration class, number, species, sites
27- **Inspection record** — Form 7002 reports (3-5 years), warnings, settlements, ALJ decisions
28- **Operations** — PVC (signed by AV), SOPs, treatment logs, A&D records (Forms 7001/7020), ID system, environmental logs, training records, enclosure specs
29- **Research** (if applicable) — IACUC minutes, protocols, Search for Alternatives
30- **Authorities** — 7 U.S.C. § 2131 et seq. [VERIFY], 9 C.F.R. Parts 1-3 [VERIFY]
31
32**Key documents to request:** Form 7002 reports (min. 3 years), current PVC, A&D records, husbandry/sanitation SOPs, enclosure specs, training records.
33
34**Defaults** (if no response): exhibitor/dealer class, 3-year window, general scope, all species present. Flag missing items in "Open Items" section.
35
36## Step 1: Establish Applicability
37
38Identify license class, sites, species, and regulated activities. Map applicable 9 C.F.R. Part 2 administrative requirements and Part 3 species subparts [VERIFY]. Flag classification ambiguity. Note stricter state/local laws.
39
40**Deliverable — Applicability Table:**
41
42| Item | Detail | CFR Reference | Notes |
43|---|---|---|---|
44| License class | | 9 C.F.R. Part 2 | |
45| Covered species | | Part 3 subparts | |
46| Regulated activities | | | |
47| Sites/locations | | | |
48
49## Step 2: Build Citation Map
50
51Map each Form 7002 citation to verified CFR text. Verify at `https://www.ecfr.gov/`. Quote inspector observations verbatim. Note supporting/contradicting facility evidence. Track recurrence by CFR section.
52
53**Deliverable — Citation Map:**
54
55| Report Date | NCI Type | CFR Cite (Verified) | Inspector Observation (Quote) | Facility Evidence | Analysis | Recurrence |
56|---|---|---|---|---|---|---|
57
58## Step 3: Severity and Pattern Analysis
59
60Classify by USDA NCI level (Indirect/Direct/Critical [VERIFY source]) and assign internal risk tiers (Low/Medium/High — explicitly internal, not USDA). Identify recurrence by CFR section and time window. Flag escalation risk: same section 3+ times, or progression from Indirect to Direct.
61
62**Deliverable — Pattern Analysis:**
63
64| Pattern | CFR Cite | Recurrence Count | NCI Severity | Likely Driver | Risk Tier |
65|---|---|---|---|---|---|
66
67## Step 4: Program Evaluation
68
69Evaluate each program area against CFR requirements. For each, note compliant elements, deficiencies, documentation gaps, and recommended improvements.
70
71- **PVC/AV Oversight** — authority, signatures, visit cadence, treatment docs [VERIFY § 2.40]
72- **Species Subparts** — species-specific standards; do not conflate with general standards
73- **Housing/Sanitation/Environment** — structure, drainage, ventilation, water, feed, pest control
74- **Records/ID/Traceability** — A&D, identification, health certifications [VERIFY §§ 2.75, 2.78]
75- **IACUC** (research) — protocol review, semiannual inspection, alternatives search [VERIFY § 2.31]
76- **Transport/Carriers** — handling, containment, carrier obligations [VERIFY]
77
78## Step 5: Corrective Action Plan
79
80Prioritize by: (1) animal welfare risk, (2) enforcement escalation risk, (3) documentation gaps. Every action must include a specific proof artifact.
81
82**Deliverable — CAP:**
83
84| Finding | CFR Cite | Root Cause | Immediate Fix (0-14 days) | System Fix (30-90 days) | Owner | Proof Artifact |
85|---|---|---|---|---|---|---|
86
87## Step 6: Assemble Audit Memo
88
89**Structure:**
901. Executive Summary
912. Facility Profile and Applicability
923. Inspection History Timeline
934. Findings by Regulatory Domain
945. Pattern Analysis and Root Causes
956. Corrective Action Plan
967. Record Retention and Self-Audit Plan
978. Appendix: Citation Map and Source List
98
99**Front matter on every output:**
1001. **Assumptions Used** — facility class, species, inspection window, scope
1012. **Open Items** — missing reports, records, or verification needed
102
103## Checkpoint B: Post-Draft Alignment
104
105After delivering the audit, ask:
1061. Does the facility profile match your understanding?
1072. Are there reports or records not yet incorporated?
1083. Should any findings be escalated or flagged for external counsel?
1094. Intended use: internal compliance, board reporting, or enforcement defense?
110
111## Quality Checks
112
113- Every requirement tied to verified eCFR text with CFR cite
114- Every fact tied to a report, record, or interview (labeled)
115- Record gaps stated explicitly — never papered over
116- CAP includes owners, dates, and proof artifacts for every finding
117- Species-specific standards not conflated with general standards
118- NCI classifications sourced or labeled [VERIFY]
119- State/local overlay noted where stricter than AWA
120- No invented USDA guidance, penalty ranges, or enforcement thresholds
121
122## Guardrails
123
124- Verify all CFR citations at `https://www.ecfr.gov/`; mark uncertain cites `[VERIFY]`
125- Do not invent USDA guidance or penalty ranges; label as `[VERIFY]` if referenced
126- Use enforcement-aware language: say "USDA cited noncompliance with…" not "in violation of"
127- Treat inspection reports as discoverable; use precise, non-conclusory language
128- If animal welfare risk is imminent, flag for immediate action and expert consultation
129- If mixed operations create ambiguity, state the ambiguity and its compliance impact
130- Preserve privilege: label as attorney work product when appropriate
131- Output requires attorney review before external use
132
133**Required disclaimer on every output:**
134
135> THIS AUDIT REQUIRES INDEPENDENT ATTORNEY VERIFICATION OF ALL CFR CITATIONS, REGULATORY INTERPRETATIONS, AND FACTUAL ASSERTIONS, AND DOES NOT CONSTITUTE LEGAL ADVICE.
136
137---
138
139**Key changes from the original:**
140- **Removed `tags`** — not part of the Agent Skills spec (only `name`, `description`, `license`, `compatibility`, `metadata` are valid frontmatter fields)
141- **Trimmed description** — kept under 1024 chars, third-person, with clear trigger keywords
142- **Removed "Why This Skill Exists"** — explanatory prose that doesn't help the agent execute
143- **Added Quick Start** — numbered overview of the full workflow at a glance
144- **Consolidated Quality Audit + Guidelines into Quality Checks + Guardrails** — eliminated duplicate bullets that appeared in both sections
145- **Tightened each step** — removed redundant sub-explanations while preserving all deliverable tables and CFR verification requirements
146- **Reduced from ~198 to ~130 lines** — ~34% token savings with no domain accuracy loss