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483
•Ivers-Lee AG•March 22, 2023

Ivers-Lee AG – FDA 483, Mar 22, 2023

Record Details

Ivers-Lee AG, a drug repacker in Burgdorf, Switzerland, was cited with two observations during an FDA inspection. The observations highlight significant deficiencies in equipment cleaning procedures, including cleaning validation and record keeping, and the accuracy and review of master production and control records. These issues indicate a lack of adequate control over critical manufacturing processes and documentation.

Company
Ivers-Lee AG
Inspection date
March 22, 2023
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Timothy Ortiz-Colon
  • Lisa Shin (Investigator)
  • David A. Oluwo (Pharmacy Intern/Certified Pharmacy Technician)
View Company Profile

ID · 339de1d3-4ecd-42a3-9603-06f4a29d4d3e

Other documents for Ivers-Lee AG
  • 483 - 2022-05-09May 9, 2022

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