Intelligence registry
Public-source dossierfda-warning-letter-d83f2f3be796e098
Official public recordorganizationRegulatory action

Dr. Thomas Balshi/Intilight

Authority: www.fda.govCoverage: GlobalPage generated: 2026-08-17
Evidence class
Official public record
Coverage
Global
Record category
Regulatory action
Page generated
2026-08-17
Linked public records

No verified ownership, offshore or transport links have been attached to this record yet.

Source and status notice
The relationship or event is sourced to a government or intergovernmental publication. Always verify the live source record and identifiers before relying on this page.

Compliance Profile

"Public-record notice: Dr. Thomas Balshi/Intilight appears in official public record data. The record is informational and should be checked against the original publisher before legal, financial or counterparty decisions are made."

Banking Impact

This public record does not establish a banking prohibition. Any onboarding or transaction decision should use the original source, a verified identity match and the institution's applicable legal framework.

Legal Status

This is an informational public record, not a sanctions, exclusion or enforcement conclusion unless the page expressly identifies an official issuing authority and record.

Public source metadata

Source: FDA Warning Letters
Full Legal NameDr. Thomas Balshi/Intilight
Known aliasesCenter for Drug Evaluation and Research | CDER / Finished Pharmaceuticals/Unapproved New Drug/Misbranded
Source datasets
FDA WARNING LETTERfda_warning_letters
Record statusInformational public record
Publishing authoritywww.fda.gov
Identifiers2022-04-13 / Finished Pharmaceuticals/Unapproved New Drug/Misbranded
Record timelineFirst seen: 2022-04-13Last seen: 2022-04-13
Risk Topicsreg.action, reg.warn, sector.medical
Original sourceView source record

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