FDA WARNING_LETTER - Trans-Missie B.V. - December 01, 2025

FDA WARNING_LETTER for Trans-Missie B.V. on December 01, 2025. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Trans-Missie B.V. 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)

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Record Information

Company

Trans-Missie B.V.

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: dc77c033-f482-416a-ad33-fd6a52e1eec7

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