FDA INVESTIGATIVE RESEARCH SYSTEM
FDA IntelDesk
LIVE DATA
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Federated FDA intelligence across inspections, enforcement, compliance actions, import actions, health fraud, product codes, recalls and public regulatory data.
DATA SOURCESInspectionsWarning LettersImport AlertsImport Refusals (FDA iRES)Health Fraud IntelligenceFDA Drug RecallsFDA Med Device RecallsFDA Food RecallsFDA Establishment Identifier (FEI)Product Code Builder
Recent FDA Warning Letters
LOADINGConnection Intelligence
READYExplainable cross-record relationship analysisConfidence combines evidence strength and independent evidence types. It is an investigative lead assessment, not a finding of identity or wrongdoing.
Runs automatically with each investigation
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Run an investigation to reveal connected records
IntelDesk compares FDA records for shared organizational, contact, location, drug, device and regulatory identifiers, then surfaces explainable relationships.
Confidence scale95–99 Confirmed Identifier80–94 Strong Match60–79 Probable40–59 Possible0–39 Weak
Exact FEI, NDC, UDI/DI, application, 510(k)/PMA, email, phone and entry-number matches carry the most weight. Generic product/substance matches are intentionally weaker. Confidence is heuristic and should be corroborated against the underlying FDA source records.
Product Identity Intelligence
READYSearch a drug, device, identifier, application, product code, or manufacturer
IntelDesk normalizes drug identity through the openFDA NDC Directory and device identity through GUDID / UDI while preserving distinct marketed products and device models.
Identity normalization is investigative context, not proof that every regulatory event concerns the exact same marketed package or device. Exact NDC, UDI/DI, application, premarket-submission and establishment identifiers should be weighted more strongly than generic product names.
Unified Results
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Search across FDA datasets using a firm, product, ingredient, location, identifier, website, or investigative keyword.
Geospatial Intelligence
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Central map layer
Run an investigation to plot location-bearing FDA records.