FDA Inspection 1205537 — Ivers-Lee AG

Ivers-Lee AG — FEI 3002420194

The FDA completed an inspection of Ivers-Lee AG on March 22, 2023 in Burgdorf. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 22, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Burgdorf (Switzerland)