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FDA Inspection 1114443 — Alk-abello A/s

Alk-abello A/s — FEI 3002806343

The FDA completed an inspection of Alk-abello A/s on November 25, 2019 in Horsholm. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 25, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Horsholm (Denmark)

Facility

Other inspections at this facility

  • 1068935 (VAI Mon Sep 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755964 (VAI Mon Nov 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources