This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
Similar Posts
FDA-TRACK: Prescription Drug User Fee Act Procedural Goals Summary
FDA-TRACK: Prescription Drug User Fee Act Procedural Goals SummaryEarly Alert: Wound and Burn Dressing Issue from Integra LifeSciences
Integra is removing all MediHoney Wound and Burn products and certain lots of CVS Wound Gel that may have breached sterile barriersDrug Safety Oversight Board
The DSB is composed of representatives from two FDA Centers and eight other federal government agencies, the Agency for Healthcare Research and Quality, Centers for Disease Control and Prevention, Centers for Medicare and Medicaid Services, Department of Defense.Petscript Inc. Paris, TX. 483 issued 09/18/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 09/18/2025
Short Title (70 char) Petscript Inc. Paris, TX. 483 issued 09/18/2025
FEI Number 3010282564
Firm Name Petscript Inc
Record Type 483
State TX
Establishment Type Producer of Sterile and Non-sterileDrug Safety and Risk Management Advisory Committee Roster
This page contains the DSARM roster, which lists the current members and the current number of vacancies for the committee.Dr. Reddy’s Laboratories, LTD, Biologics – 09/12/2025
Dr. Reddy’s Laboratories, LTD, Biologics – 09/12/2025. Country: India. Record Type: 483