Anti-biofilm Technologies for Enhancing the Safety of Medical Device Surfaces, May 29, 2025.
Similar Posts
Boothwyn Pharmacy LLC. Kennett Square, PA. 483 issued 06/09/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 06/09/2025
Short Title (70 char) Boothwyn Pharmacy LLC. Kennett Square, PA. 483 issued 06/09/2025
FEI Number 1000076625
Firm Name Boothwyn Pharmacy LLC
Record Type 483
State PA
Establishment Type Producer of SteKroger Voluntarily Recalls Two Varieties of Deli Pasta Salads Because of Possible Health Risk
CINCINNATI, October 4, 2025 – The Kroger Co. (NYSE: KR), said today it has recalled Basil Pesto Bowtie Salad and Smoked Mozzarella Penne Salad that was sold in the Kroger Family of Stores in following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SCFDA Adverse Event Reporting System (FAERS) Public Dashboard
Four FAERS summary statistics reports updated with data through December 31, 2013.MedWatch: The FDA Safety Information and Adverse Event Reporting Program
MedWatch is made up of voluntary and mandatory reporting on prescription medicines, over-the-counter medicines, non-vaccine biologicals, medical devices, special nutritional products, cosmetics and non-prescription human drug products marketed without an approved application.Drug Development Tool Qualification Process: Transparency Provisions
Under the 21st Century Cures Act enacted on December 13, 2016, the new section 507 Qualification of Drug Development Tools was added to the Federal Food, Drug, and Cosmetic Act and formally establishes an updated, multi-stage process for DDT qualification. This process includes three submission milHetero Labs Limited, Unit-IX – 09/26/2025
Hetero Labs Limited, Unit-IX – 09/26/2025. Country: India. Record Type: 483