The screenshot shows the /audit/[id] page with a risk score gauge (6.0), OCR confidence bar, AI summary with regulation references, FDA history checks (all empty), extracted product info (brand, name, ingredients), and the beginning of CFR compliance detail cards. Let me deeply analyze the components.

Let me continue the deep analysis. I need to read the remaining parts of the audit result view and all related components:

Now let me check the remaining sections - the violation section cards, the expert-request-panel, and the pricing page to understand what conversions need to happen:

Now let me also check the preview page (paywall), the i18n strings for report-related translations, and the ViolationCard component used in the inline layout:

Now let me check what data fields are available but NOT being shown in the report-result-view:

Now let me check the DB fields available that are NOT used:

Let me also see the remaining schema and read the more recent schema additions:

Let me also check the later migration scripts for newer fields:

Now I have a comprehensive picture. Let me also check what i18n keys exist for report to plan new ones:

Now I have a comprehensive understanding of all components. Let me write the plan: