FDA WARNING_LETTER - TOMSCOUT - December 01, 2025

FDA WARNING_LETTER for TOMSCOUT on December 01, 2025. Product: Devices. Access full analysis and detailed observations.

One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.

Record Summary

FDA WARNING_LETTER for TOMSCOUT on December 01, 2025. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 U.S.C. 360(j)

FD&C Act 510(p)

FD&C Act 502(o)

21 U.S.C. 360(p)

21 U.S.C. 360

FD&C Act 201(h)

21 U.S.C. 321(h)

FD&C Act 510

FD&C Act 510(j)

21 U.S.C. 352(o)

Get More Insights

Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.

1.5M+ regulatory data points

Real-time compliance monitoring

Interactive analytics dashboard

Looking for more records? Our platform provides access to thousands of similar regulatory documents with advanced search and filtering capabilities.

Record Information

Company

TOMSCOUT

Inspection Date

December 1, 2025

Product Type

Devices

Office

Office of Health Technology 3 (Gastrorenal, ObGyn, General Hospital, and Urology Devices)

People

Michael J. Hoffmann

ID: b7a59b30-181e-46fd-8e8b-ad6093525bc7

View on Dashboard

Transform Regulatory Data into Actionable Intelligence

Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.

Try KeyPedia Today

Explore our real use cases and discover our features in depth.

Subscribe to our newsletter

Get the latest updates and insights delivered to your inbox