Medtech Insight is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

US FDA Now Assessing UDI Compliance When Inspecting Device Firms

This article was originally published in SRA

Executive Summary

Unique device identification (UDI) activities are now being reviewed by US Food and Drug Administration investigators during medical device facility inspections, an agency official says. In addition, firms that aren't required yet to abide by the UDI regulation will be quizzed about their preparedness.

Advertisement
Advertisement
UsernamePublicRestriction

Register

MT040646

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

All set! This Question has been sent to my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel