fda_manufacturing_risk_summary
ActiveTool of FDA Data MCP
declared in 0.1.0
Build a manufacturing and compliance summary for one company using FDA facilities, inspections, warning letters, OII records, import-risk signals, debarments, and recalls. Use this when you want the company-level picture first, then follow the linked granular tools for deeper inspection.
Parameters schema
{
"type": "object",
"$schema": "http://json-schema.org/draft-07/schema#",
"required": [
"company"
],
"properties": {
"company": {
"type": "string",
"maxLength": 500,
"description": "Company name to summarize"
},
"verbose": {
"type": "boolean",
"default": false,
"description": "When false (default), suppress the inline alias dump and collapse per-dataset data_freshness to a single top-level as_of. Set true for the full block."
},
"evidence_limit": {
"type": "integer",
"default": 5,
"maximum": 25,
"minimum": 1,
"description": "Max recent records to return per evidence section"
},
"facility_limit": {
"type": "integer",
"default": 10,
"maximum": 50,
"minimum": 1,
"description": "Max facilities to return"
}
}
}No endpoints wrapped at confidence ≥ 0.70.
Parent server
FDA Data MCP
https://github.com/medley/fda-data
1/7 registries